homozygots.txt

Start getting SNPs from snpedia.com
Got 22949 SNPs from snpedia.com

Start getting SNPs from user
Got 966983 SNPs from user

Start filtering SNPs
Got 8600 SNPs that are available on SNPedia & are homozygotous

Start getting genotypes
Got 8410 SNPs from SNPedia which have known genotypes

Start getting genotype descriptions
Got 2245 genotypes with a sufficient description

Start getting relevant genotypes

1
-----------
My genotype at rs6684865: GG or (G;G)
rs6684865(A;A) is associated with: 1.5x risk
rs6684865(A;G) is associated with: 1.2x risk
rs6684865(G;G) is associated with: normal

2
-----------
My genotype at rs3890745: TT or (A;A)
rs3890745(A;A) is associated with: 1.12x risk of Rheumatoid arthritis
rs3890745(A;G) is associated with: 
rs3890745(G;G) is associated with: normal

3
-----------
My genotype at rs17376328: GG or (G;G)
rs17376328(A;A) is associated with: lower blood pressure
rs17376328(A;G) is associated with: lower blood pressure
rs17376328(G;G) is associated with: normal

4
-----------
My genotype at rs198358: TT or (A;A)
rs198358(A;A) is associated with: normal
rs198358(A;G) is associated with: lower blood pressure
rs198358(G;G) is associated with: lower blood pressure

5
-----------
My genotype at rs5067: AA or (A;A)
rs5067(A;A) is associated with: normal
rs5067(A;G) is associated with: 0.5x reduced risk for asthma
rs5067(G;G) is associated with: 0.5x reduced risk for asthma

6
-----------
My genotype at rs5065: AA or (A;A)
rs5065(A;A) is associated with: 1.12x risk on diuretic; if hypertensive, better outcome when treated with calcium channel blocker than with diuretic
rs5065(A;G) is associated with: normal risk
rs5065(G;G) is associated with: 0.87x risk on diuretic; if hypertensive, better outcome when treated with diuretic than with calcium channel blocker

7
-----------
My genotype at rs7543472: TT or (T;T)
rs7543472(C;C) is associated with: normal
rs7543472(C;T) is associated with: weakly associated with increased cataract risk
rs7543472(T;T) is associated with: ~2x increased risk for cataracts

8
-----------
My genotype at rs2240340: TT or (A;A)
rs2240340(A;A) is associated with: increased risk for RA
rs2240340(A;G) is associated with: increased risk for RA
rs2240340(G;G) is associated with: average

9
-----------
My genotype at rs11809207: GG or (G;G)
rs11809207(A;A) is associated with: 0.92cm taller on average
rs11809207(A;G) is associated with: 0.46cm taller on average
rs11809207(G;G) is associated with: normal

10
-----------
My genotype at rs5800: CC or (G;G)
rs5800(A;A) is associated with: AF risk in HCM patients (only)
rs5800(A;G) is associated with: AF risk in HCM patients (only)
rs5800(G;G) is associated with: normal

11
-----------
My genotype at rs36053993: CC or (G;G)
rs36053993(A;A) is associated with: increased risk for certain cancers?
rs36053993(A;G) is associated with: increased risk for certain cancers?
rs36053993(G;G) is associated with: normal

12
-----------
My genotype at rs34612342: TT or (A;A)
rs34612342(A;A) is associated with: normal
rs34612342(A;G) is associated with: increased risk for certain cancers?
rs34612342(G;G) is associated with: increased risk for certain cancers?

13
-----------
My genotype at rs324420: AA or (A;A)
rs324420(A;A) is associated with: significantly increased risk for substance use disorders
rs324420(A;C) is associated with: normal
rs324420(C;C) is associated with: normal

14
-----------
My genotype at rs8179183: GG or (G;G)
rs8179183(C;C) is associated with: normal
rs8179183(C;G) is associated with: less likely to gain weight if taking risperidone
rs8179183(G;G) is associated with: less likely to gain weight if taking risperidone

15
-----------
My genotype at rs1892534: CC or (G;G)
rs1892534(A;A) is associated with: 1.2x increased risk overall for cancers
rs1892534(G;G) is associated with: normal

16
-----------
My genotype at rs4655595: AA or (A;A)
rs4655595(A;A) is associated with: normal
rs4655595(A;G) is associated with: 1.4 risk
rs4655595(G;G) is associated with: 2.3 risk

17
-----------
My genotype at rs11465770: CC or (C;C)
rs11465770(C;C) is associated with: normal Crohn's Disease risk
rs11465770(C;T) is associated with: possibly lower risk of Crohn's Disease (OR=0.30)
rs11465770(T;T) is associated with: possibly lower risk of Crohn's Disease (OR=0.30)

18
-----------
My genotype at rs7530511: CC or (C;C)
rs7530511(C;C) is associated with: normal
rs7530511(C;T) is associated with: normal
rs7530511(T;T) is associated with: 9x increased risk for Graves disease

19
-----------
My genotype at rs11465804: TT or (T;T)
rs11465804(G;G) is associated with: 0.68x lower risk for spondylitis
rs11465804(G;T) is associated with: 0.68x lower risk for spondylitis
rs11465804(T;T) is associated with: normal risk

20
-----------
My genotype at rs11209026: GG or (G;G)
rs11209026(A;A) is associated with: 0.26x lower risk for certain autoimmune diseases
rs11209026(A;G) is associated with: 0.26x lower risk for certain autoimmune diseases
rs11209026(G;G) is associated with: common

21
-----------
My genotype at rs1343151: GG or (C;C)
rs1343151(C;C) is associated with: normal risk
rs1343151(C;T) is associated with: 0.8x lower risk for spondylitis
rs1343151(T;T) is associated with: 0.8x lower risk for spondylitis

22
-----------
My genotype at rs10889677: AA or (A;A)
rs10889677(A;A) is associated with: 1.5x risk for certain autoimmune diseases
rs10889677(A;C) is associated with: 1.5x risk for certain autoimmune diseases; 2x risk for Graves disease
rs10889677(C;C) is associated with: 1x risk for certain autoimmune diseases; 2.3x risk for Graves disease

23
-----------
My genotype at rs12567232: AA or (A;A)
rs12567232(A;A) is associated with: Increased risk for Crohn's Disease
rs12567232(A;G) is associated with: Increased risk for Crohn's Disease
rs12567232(G;G) is associated with: normal

24
-----------
My genotype at rs11209032: AA or (A;A)
rs11209032(A;A) is associated with: 1.3x higher risk for spondylitis
rs11209032(A;G) is associated with: 1.3x higher risk for spondylitis
rs11209032(G;G) is associated with: normal risk

25
-----------
My genotype at rs1495965: CC or (G;G)
rs1495965(A;A) is associated with: 1.2x higher risk for spondylitis
rs1495965(A;G) is associated with: 1.2x higher risk for spondylitis
rs1495965(G;G) is associated with: normal risk

26
-----------
My genotype at rs527974: GG or (C;C)
rs527974(C;C) is associated with: better response to certain calcium channel blockers
rs527974(C;T) is associated with: better response to certain calcium channel blockers
rs527974(T;T) is associated with: normal

27
-----------
My genotype at rs11162922: AA or (A;A)
rs11162922(A;A) is associated with: 2x risk
rs11162922(A;G) is associated with: 1.3x risk
rs11162922(G;G) is associated with: normal

28
-----------
My genotype at rs10735781: CC or (G;G)
rs10735781(C;C) is associated with: >1.11x risk
rs10735781(C;G) is associated with: 1.11x risk
rs10735781(G;G) is associated with: common

29
-----------
My genotype at rs6680578: AA or (T;T)
rs6680578(A;A) is associated with: >1.11x risk
rs6680578(A;T) is associated with: 1.11x risk
rs6680578(T;T) is associated with: common

30
-----------
My genotype at rs6604026: TT or (T;T)
rs6604026(C;C) is associated with: >1.15x risk
rs6604026(C;T) is associated with: 1.15x risk
rs6604026(T;T) is associated with: common

31
-----------
My genotype at rs7536563: GG or (G;G)
rs7536563(A;A) is associated with: >1.12x risk
rs7536563(A;G) is associated with: 1.12x risk
rs7536563(G;G) is associated with: common

32
-----------
My genotype at rs3918290: CC or (G;G)
rs3918290(A;A) is associated with: 5-fluorouracil toxicity
rs3918290(A;G) is associated with: some 5-fluorouracil toxicity 

33
-----------
My genotype at rs12021720: CC or (C;C)
rs12021720(T;T) is associated with: rare genotype but harmless

34
-----------
My genotype at rs1676486: GG or (G;G)
rs1676486(A;A) is associated with: >1.4x risk for LDH
rs1676486(A;G) is associated with: 1.4x risk for LDH

35
-----------
My genotype at rs646776: TT or (A;A)
rs646776(A;A) is associated with: 1.2x risk of coronary artery disease

36
-----------
My genotype at rs599839: AA or (A;A)
rs599839(A;A) is associated with: 1.29x increased risk for heart disease
rs599839(A;G) is associated with: 1.29x increased risk for heart disease
rs599839(G;G) is associated with: normal

37
-----------
My genotype at rs6679677: CC or (C;C)
rs6679677(A;A) is associated with: 5.2x risk for T1D; 3.3x for RA
rs6679677(A;C) is associated with: 1.8x risk for T1D; 2x risk for RA
rs6679677(C;C) is associated with: normal

38
-----------
My genotype at rs3789604: TT or (T;T)
rs3789604(G;G) is associated with: 1.7x increased RA risk
rs3789604(G;T) is associated with: 1.5x increased RA risk; 1.4x increased GD risk
rs3789604(T;T) is associated with: normal for RA; 1.4x increased GD risk

39
-----------
My genotype at rs2476601: GG or (G;G)
rs2476601(A;A) is associated with: rare genotype
rs2476601(A;G) is associated with: 2x risk for T1D, RA, Addison's
rs2476601(G;G) is associated with: normal

40
-----------
My genotype at rs17602729: GG or (G;G)
rs17602729(A;A) is associated with: AMPD1 deficiency
rs17602729(A;G) is associated with: AMPD1 heterozygote
rs17602729(G;G) is associated with: common

41
-----------
My genotype at rs6330: GG or (C;C)
rs6330(C;C) is associated with: more anxious females, less anxious males
rs6330(C;T) is associated with: normal
rs6330(T;T) is associated with: more anxious males, less anxious females

42
-----------
My genotype at rs12044852: CC or (C;C)
rs12044852(A;A) is associated with: common
rs12044852(A;C) is associated with: 1.24x risk
rs12044852(C;C) is associated with: >1.24x risk

43
-----------
My genotype at rs10754339: AA or (A;A)
rs10754339(A;A) is associated with: normal
rs10754339(A;G) is associated with: 1.3x increased risk of breast cancer
rs10754339(G;G) is associated with: 1.45x increased risk of breast cancer

44
-----------
My genotype at rs10801935: AA or (A;A)
rs10801935(A;A) is associated with: normal
rs10801935(A;C) is associated with: normal
rs10801935(C;C) is associated with: 0.3x decreased risk of breast cancer

45
-----------
My genotype at rs3738414: GG or (G;G)
rs3738414(A;A) is associated with: 0.4x decreased risk of breast cancer
rs3738414(A;G) is associated with: normal
rs3738414(G;G) is associated with: normal

46
-----------
My genotype at rs2145418: AA or (T;T)
rs2145418(G;G) is associated with: 9.2x increased thyroid cancer risk
rs2145418(G;T) is associated with: 5.0x increased thyroid cancer risk
rs2145418(T;T) is associated with: normal

47
-----------
My genotype at rs17646946: GG or (G;G)
rs17646946(A;A) is associated with: straighter curl

48
-----------
My genotype at rs11803731: AA or (T;T)
rs11803731(A;A) is associated with: straighter hair
rs11803731(T;T) is associated with: curlier hair

49
-----------
My genotype at rs499697: AA or (T;T)
rs499697(T;T) is associated with: straighter hair

50
-----------
My genotype at rs6684439: TT or (T;T)
rs6684439(C;C) is associated with: normal
rs6684439(C;T) is associated with: 1.7x increased melanoma risk
rs6684439(T;T) is associated with: normal?

51
-----------
My genotype at rs4845618: TT or (T;T)
rs4845618(G;G) is associated with: normal
rs4845618(G;T) is associated with: 1.7x increased melanoma risk
rs4845618(T;T) is associated with: normal?

52
-----------
My genotype at rs8192284: CC or (C;C)
rs8192284(A;A) is associated with: normal
rs8192284(A;C) is associated with: 1.7x increased melanoma risk
rs8192284(C;C) is associated with: normal?

53
-----------
My genotype at rs13376333: CC or (C;C)
rs13376333(C;T) is associated with: 1.5x higher risk of atrial fibrillation
rs13376333(T;T) is associated with: ~2x higher risk of atrial fibrillation

54
-----------
My genotype at rs2230288: CC or (G;G)
rs2230288(A;A) is associated with: Homozygous for E326K variant of GBA gene
rs2230288(A;G) is associated with: E326K variant in GBA gene

55
-----------
My genotype at rs364897: TT or (A;A)
rs364897(A;G) is associated with: N188S variant of the GBA gene
rs364897(G;G) is associated with: Homozygous for N188S variant of GBA gene

56
-----------
My genotype at rs2297480: GG or (C;C)
rs2297480(A;A) is associated with: normal
rs2297480(A;C) is associated with: normal
rs2297480(C;C) is associated with: reduced response to anti-osteoporosis drugs

57
-----------
My genotype at rs2814778: TT or (A;A)
rs2814778(A;A) is associated with: Duffy-positive
rs2814778(A;G) is associated with: Duffy-positive
rs2814778(G;G) is associated with: Duffy-negative: increased odds of HIV infection upon exposure, but slowed disease progression if infected

58
-----------
My genotype at rs2427837: GG or (G;G)
rs2427837(A;A) is associated with: lowest IgE levels
rs2427837(A;G) is associated with: lower IgE levels
rs2427837(G;G) is associated with: normal but highest IgE levels

59
-----------
My genotype at rs2251746: TT or (T;T)
rs2251746(C;C) is associated with: lowest IgE levels
rs2251746(C;T) is associated with: lower IgE levels
rs2251746(T;T) is associated with: normal but highest IgE levels

60
-----------
My genotype at rs1800947: CC or (G;G)
rs1800947(C;C) is associated with: lower CRP levels
rs1800947(C;G) is associated with: lower CRP levels
rs1800947(G;G) is associated with: normal

61
-----------
My genotype at rs3766379: TT or (T;T)
rs3766379(C;C) is associated with: normal
rs3766379(C;T) is associated with: 1.37x increased risk for rheumatoid arthritis
rs3766379(T;T) is associated with: 1.9x increased risk for rheumatoid arthritis

62
-----------
My genotype at rs6682654: GG or (G;G)
rs6682654(A;G) is associated with: 1.34x increased risk for rheumatoid arthritis
rs6682654(G;G) is associated with: 1.8x increased risk for rheumatoid arthritis

63
-----------
My genotype at rs1801274: AA or (T;T)
rs1801274(C;C) is associated with: normal
rs1801274(C;T) is associated with: complex; generally greater risk for cancer progression
rs1801274(T;T) is associated with: complex; generally greater risk for cancer progression

64
-----------
My genotype at rs10918594: GG or (G;G)
rs10918594(C;C) is associated with: Shorter QT interval
rs10918594(C;G) is associated with: average QT interval
rs10918594(G;G) is associated with: Longer QT interval

65
-----------
My genotype at rs4656461: AA or (A;A)
rs4656461(A;A) is associated with: normal
rs4656461(A;G) is associated with: 1.5x increased risk for open angle glaucoma
rs4656461(G;G) is associated with: 2.2x increased risk for open angle glaucoma

66
-----------
My genotype at rs6025: CC or (G;G)
rs6025(A;A) is associated with: Prone to thrombosis
rs6025(A;G) is associated with: Prone to thrombosis
rs6025(G;G) is associated with: normal/common

67
-----------
My genotype at rs5361: TT or (A;A)
rs5361(A;A) is associated with: normal risk
rs5361(A;C) is associated with: normal risk
rs5361(C;C) is associated with: 4x increased risk for recurrent venous thromboembolism.

68
-----------
My genotype at rs12037606: GG or (G;G)
rs12037606(A;A) is associated with: 1.5x risk of Crohn's disease
rs12037606(A;G) is associated with: 1.2x risk of Crohn's disease
rs12037606(G;G) is associated with: normal

69
-----------
My genotype at rs486907: TT or (A;A)
rs486907(A;A) is associated with: 2x increased prostate cancer risk
rs486907(A;G) is associated with: 1.5x increased prostate cancer risk
rs486907(G;G) is associated with: normal

70
-----------
My genotype at rs3738579: GG or (C;C)
rs3738579(C;C) is associated with: 1.5x increased risk for breast cancer, HNSCC
rs3738579(C;T) is associated with: 0.5x decreased risk for several cancers
rs3738579(T;T) is associated with: 1.3x - 2x increased risk for several cancers

71
-----------
My genotype at rs5275: AA or (T;T)
rs5275(C;C) is associated with: 0.68x decreased risk for bladder cancer
rs5275(C;T) is associated with: 0.68x decreased risk for bladder cancer
rs5275(T;T) is associated with: normal

72
-----------
My genotype at rs2745557: GG or (G;G)
rs2745557(A;A) is associated with: autism risk?
rs2745557(A;G) is associated with: autism risk?
rs2745557(G;G) is associated with: normal

73
-----------
My genotype at rs20417: CC or (G;G)
rs20417(C;C) is associated with: normal risk of diabetes
rs20417(C;G) is associated with: 30% higher risk of diabetes
rs20417(G;G) is associated with: ?

74
-----------
My genotype at rs689465: TT or (A;A)
rs689465(A;A) is associated with: 1.5x increased risk for mild asthma
rs689465(A;G) is associated with: slight increased risk for mild asthma
rs689465(G;G) is associated with: normal

75
-----------
My genotype at rs800292: GG or (C;C)
rs800292(C;C) is associated with: normal
rs800292(C;T) is associated with: increased risk of macular degeneration
rs800292(T;T) is associated with: increased risk of macular degeneration

76
-----------
My genotype at rs1061170: CC or (C;C)
rs1061170(C;C) is associated with: 5.9x risk for AMD; higher mortality among nonagenarians
rs1061170(C;T) is associated with: 2.5x risk for AMD; higher mortality among nonagenarians
rs1061170(T;T) is associated with: common/normal

77
-----------
My genotype at rs380390: GG or (G;G)
rs380390(C;C) is associated with: increased risk for ARMD
rs380390(C;G) is associated with: None

78
-----------
My genotype at rs1329428: CC or (G;G)
rs1329428(A;A) is associated with: normal
rs1329428(A;G) is associated with: ?
rs1329428(G;G) is associated with: 2x increased risk for macular degeneration

79
-----------
My genotype at rs7539542: GG or (G;G)
rs7539542(C;C) is associated with: 0.51x decreased breast cancer risk
rs7539542(C;G) is associated with: 0.59x decreased breast cancer risk
rs7539542(G;G) is associated with: normal

80
-----------
My genotype at rs642961: GG or (G;G)
rs642961(A;A) is associated with: normal
rs642961(A;G) is associated with: 1.9x risk of cleft lip
rs642961(G;G) is associated with: 2.3x risk of cleft lip

81
-----------
My genotype at rs2639703: TT or (T;T)
rs2639703(C;C) is associated with: 1.6x risk
rs2639703(C;T) is associated with: 1.1x risk
rs2639703(T;T) is associated with: normal

82
-----------
My genotype at rs1136410: AA or (T;T)
rs1136410(C;C) is associated with: 0.80x reduced risk for glioblastoma
rs1136410(C;T) is associated with: 0.80x reduced risk for glioblastoma
rs1136410(T;T) is associated with: normal

83
-----------
My genotype at rs6675281: CC or (C;C)
rs6675281(C;C) is associated with: common
rs6675281(C;T) is associated with: None
rs6675281(T;T) is associated with: None

84
-----------
My genotype at rs2820037: AA or (T;T)
rs2820037(A;A) is associated with: normal
rs2820037(A;T) is associated with: 1.5x risk
rs2820037(T;T) is associated with: 1.1x risk

85
-----------
My genotype at rs4481887: GG or (G;G)
rs4481887(A;A) is associated with: 74% of you can smell asparagus metabolites in urine
rs4481887(A;G) is associated with: 71% of you can smell asparagus metabolites in urine
rs4481887(G;G) is associated with: 57%% of you can smell asparagus metabolites in urine

86
-----------
My genotype at rs10192566: GG or (G;G)
rs10192566(C;C) is associated with: if diabetic, poorer response to rosiglitazone
rs10192566(C;G) is associated with: if diabetic, better response to rosiglitazone
rs10192566(G;G) is associated with: if diabetic, better response to rosiglitazone

87
-----------
My genotype at rs10495584: AA or (A;A)
rs10495584(A;A) is associated with: normal
rs10495584(A;G) is associated with: lower blood pressure
rs10495584(G;G) is associated with: lower blood pressure

88
-----------
My genotype at rs5742904: CC or (G;G)
rs5742904(A;A) is associated with: Hypercholesterolemia, Type B; homozygote
rs5742904(A;G) is associated with: Hypercholesterolemia, Type B; heterozygote
rs5742904(G;G) is associated with: normal

89
-----------
My genotype at rs520354: AA or (A;A)
rs520354(A;A) is associated with: increased risk in men for biliary conditions
rs520354(A;G) is associated with: increased risk in men for biliary conditions
rs520354(G;G) is associated with: normal

90
-----------
My genotype at rs7577363: GG or (G;G)
rs7577363(A;A) is associated with: >1.37x risk
rs7577363(A;G) is associated with: 1.37x risk
rs7577363(G;G) is associated with: common

91
-----------
My genotype at rs9332964: CC or (G;G)
rs9332964(A;A) is associated with: micropenis
rs9332964(A;G) is associated with: average
rs9332964(G;G) is associated with: average

92
-----------
My genotype at rs1126497: TT or (T;T)
rs1126497(C;C) is associated with: normal
rs1126497(C;T) is associated with: 1.4x increased risk for breast cancer
rs1126497(T;T) is associated with: 1.4x increased risk for breast cancer

93
-----------
My genotype at rs10865331: AA or (A;A)
rs10865331(A;A) is associated with: 1.4x higher risk for ankylosing spondylitis
rs10865331(A;G) is associated with: 1.2x higher risk for ankylosing spondylitis
rs10865331(G;G) is associated with: normal

94
-----------
My genotype at rs721048: GG or (G;G)
rs721048(A;A) is associated with: slightly increased prostate cancer risk
rs721048(A;G) is associated with: None
rs721048(G;G) is associated with: normal

95
-----------
My genotype at rs12469063: AA or (A;A)
rs12469063(A;A) is associated with: >1.7x risk for restless legs
rs12469063(A;G) is associated with: 1.7x risk for restless legs
rs12469063(G;G) is associated with: common

96
-----------
My genotype at rs2300478: TT or (T;T)
rs2300478(G;G) is associated with: >1.7x risk for restless legs
rs2300478(G;T) is associated with: 1.7x risk for restless legs
rs2300478(T;T) is associated with: common

97
-----------
My genotype at rs1007371: TT or (T;T)
rs1007371(T;T) is associated with: rare genotype.

98
-----------
My genotype at rs2278206: AA or (T;T)
rs2278206(C;C) is associated with: 1.16x increased risk for asthma
rs2278206(C;T) is associated with: normal
rs2278206(T;T) is associated with: possibly less susceptible to asthma

99
-----------
My genotype at rs7570682: GG or (G;G)
rs7570682(A;A) is associated with: 1.6x risk
rs7570682(A;G) is associated with: 1.2x risk
rs7570682(G;G) is associated with: normal

100
-----------
My genotype at rs3827760: AA or (T;T)
rs3827760(C;C) is associated with: shovel-Shaped Incisors

101
-----------
My genotype at rs1800587: GG or (C;C)
rs1800587(C;C) is associated with: normal
rs1800587(C;T) is associated with: normal
rs1800587(T;T) is associated with: increased waist circumference and risk of disk disease

102
-----------
My genotype at rs1143634: GG or (C;C)
rs1143634(C;C) is associated with: normal
rs1143634(C;T) is associated with: complex; see details
rs1143634(T;T) is associated with: complex; see details

103
-----------
My genotype at rs419598: TT or (T;T)
rs419598(C;C) is associated with: 0.29x lower risk for periodontitis
rs419598(C;T) is associated with: 0.29x lower risk for periodontitis
rs419598(T;T) is associated with: normal

104
-----------
My genotype at rs1375144: GG or (C;C)
rs1375144(C;C) is associated with: 1.6x risk
rs1375144(C;T) is associated with: 1.3x risk
rs1375144(T;T) is associated with: normal

105
-----------
My genotype at rs2069912: CC or (C;C)
rs2069912(C;C) is associated with: sepsis risk in East Asians
rs2069912(C;T) is associated with: sepsis risk in East Asians
rs2069912(T;T) is associated with: normal

106
-----------
My genotype at rs4988235: AA or (T;T)
rs4988235(C;C) is associated with: possibly lactose intolerant
rs4988235(C;T) is associated with: can digest milk
rs4988235(T;T) is associated with: can digest milk

107
-----------
My genotype at rs182549: TT or (T;T)
rs182549(C;C) is associated with: possibly lactose intolerant
rs182549(C;T) is associated with: None
rs182549(T;T) is associated with: None

108
-----------
My genotype at rs3754777: CC or (G;G)
rs3754777(A;A) is associated with: slightly higher blood pressure if Caucasian
rs3754777(A;G) is associated with: slightly higher blood pressure if Caucasian
rs3754777(G;G) is associated with: normal

109
-----------
My genotype at rs6749447: TT or (T;T)
rs6749447(G;G) is associated with: slightly higher blood pressure if Caucasian
rs6749447(G;T) is associated with: slightly higher blood pressure if Caucasian
rs6749447(T;T) is associated with: normal

110
-----------
My genotype at rs573225: AA or (T;T)
rs573225(C;C) is associated with: normal
rs573225(C;T) is associated with: higher insulinogenic index in obese children
rs573225(T;T) is associated with: higher insulinogenic index in obese children

111
-----------
My genotype at rs1344706: CC or (G;G)
rs1344706(G;G) is associated with: normal
rs1344706(G;T) is associated with: 1.1x increased risk for schizophrenia
rs1344706(T;T) is associated with: 1.2x increased risk for schizophrenia

112
-----------
My genotype at rs1800255: GG or (G;G)
rs1800255(A;A) is associated with: increased risk for pelvic organ prolapse
rs1800255(A;G) is associated with: normal
rs1800255(G;G) is associated with: normal

113
-----------
My genotype at rs3821236: GG or (G;G)
rs3821236(A;A) is associated with: 2x higher risk of lupus
rs3821236(A;G) is associated with: 1.4x higher risk of lupus

114
-----------
My genotype at rs7574865: GG or (G;G)
rs7574865(G;G) is associated with: common
rs7574865(G;T) is associated with: 1.3x risk for RA; 1.5x for SLE
rs7574865(T;T) is associated with: 2x risk for RA; 1.6x for SLE; 1.9x increased risk for type-1 diabetes

115
-----------
My genotype at rs10181656: CC or (G;G)
rs10181656(C;C) is associated with: normal
rs10181656(C;G) is associated with: 1.7x increased SLE risk
rs10181656(G;G) is associated with: 1.7x increased SLE risk

116
-----------
My genotype at rs7582694: GG or (G;G)
rs7582694(C;C) is associated with: 1.71x increased SLE risk
rs7582694(C;G) is associated with: 1.71x increased SLE risk
rs7582694(G;G) is associated with: normal

117
-----------
My genotype at rs700651: AA or (A;A)
rs700651(A;A) is associated with: normal
rs700651(A;G) is associated with: ~1.18x increased risk of aneurysm
rs700651(G;G) is associated with: ~1.56x increased risk of aneurysm

118
-----------
My genotype at rs828907: GG or (G;G)
rs828907(G;G) is associated with: normal
rs828907(G;T) is associated with: slightly increased risk of bladder cancer
rs828907(T;T) is associated with: slightly increased risk of bladder cancer

119
-----------
My genotype at rs2059693: CC or (C;C)
rs2059693(C;C) is associated with: normal
rs2059693(C;T) is associated with: 1.3x increased risk for testicular cancer
rs2059693(T;T) is associated with: 1.6x increased risk for testicular cancer

120
-----------
My genotype at rs1801278: CC or (G;G)
rs1801278(A;A) is associated with: reduced colorectal risk when combined with INSR SNP
rs1801278(A;G) is associated with: reduced colorectal risk when combined with INSR SNP
rs1801278(G;G) is associated with: normal

121
-----------
My genotype at rs10210302: TT or (T;T)
rs10210302(C;C) is associated with: normal
rs10210302(C;T) is associated with: 1.2x risk
rs10210302(T;T) is associated with: 1.8x risk

122
-----------
My genotype at rs2241880: GG or (C;C)
rs2241880(C;C) is associated with: 2x-3x increased risk for Crohn's disease in Caucasians
rs2241880(C;T) is associated with: 1.4x increased risk for Crohn's disease in Caucasians
rs2241880(T;T) is associated with: normal

123
-----------
My genotype at rs58597806: GG or (G;G)
rs58597806(G;G) is associated with: normal
rs58597806(G;T) is associated with: likely reduced UGT1A9 glucuronidation
rs58597806(T;T) is associated with: likely reduced UGT1A9 glucuronidation

124
-----------
My genotype at rs4148323: GG or (G;G)
rs4148323(A;A) is associated with: homozygous for UGT1A1*6
rs4148323(A;G) is associated with: carrier of 1 UGT1A1*6 allele
rs4148323(G;G) is associated with: normal

125
-----------
My genotype at rs2953145: CC or (G;G)
rs2953145(C;C) is associated with: normal
rs2953145(C;G) is associated with: 1.8x risk
rs2953145(G;G) is associated with: 2.1x risk

126
-----------
My genotype at rs1052133: CC or (G;G)
rs1052133(C;C) is associated with: normal
rs1052133(C;G) is associated with: normal for bladder cancer risk; 1.9x increased risk for gallbladder cancer
rs1052133(G;G) is associated with: 2x increased bladder cancer risk; 4.5x increased risk for gallbladder cancer

127
-----------
My genotype at rs17036314: GG or (G;G)
rs17036314(C;C) is associated with: risk of progressing from IGT to T2D; reduced by exercise
rs17036314(C;G) is associated with: risk of progressing from IGT to T2D; reduced by exercise
rs17036314(G;G) is associated with: normal

128
-----------
My genotype at rs1801282: CC or (G;G)
rs1801282(C;G) is associated with: watch out for high fat in diet
rs1801282(G;G) is associated with: watch out for high fat in diet

129
-----------
My genotype at rs2228001: TT or (A;A)
rs2228001(A;A) is associated with: statistically significant, but slight, increase in lung cancer risk
rs2228001(A;C) is associated with: normal
rs2228001(C;C) is associated with: normal

130
-----------
My genotype at rs2228000: GG or (C;C)
rs2228000(C;C) is associated with: normal
rs2228000(C;T) is associated with: normal
rs2228000(T;T) is associated with: statistically significant, but slight, increase in bladder cancer risk

131
-----------
My genotype at rs7639618: CC or (C;C)
rs7639618(C;C) is associated with: normal
rs7639618(C;T) is associated with: 1.45x increased osteoarthritis risk
rs7639618(T;T) is associated with: 1.45x increased osteoarthritis risk

132
-----------
My genotype at rs11718863: AA or (T;T)
rs11718863(A;A) is associated with: normal
rs11718863(A;T) is associated with: 1.43x increased osteoarthritis risk
rs11718863(T;T) is associated with: 1.43x increased osteoarthritis risk

133
-----------
My genotype at rs4399848: GG or (G;G)
rs4399848(A;A) is associated with: rare
rs4399848(A;G) is associated with: Heterozygous
rs4399848(G;G) is associated with: normal

134
-----------
My genotype at rs4276227: TT or (T;T)
rs4276227(C;C) is associated with: 1.5x risk
rs4276227(C;T) is associated with: 1.2x risk
rs4276227(T;T) is associated with: normal

135
-----------
My genotype at rs3732379: CC or (C;C)
rs3732379(T;T) is associated with: increased susceptibility

136
-----------
My genotype at rs312481: GG or (C;C)
rs312481(C;C) is associated with: better response to certain calcium channel blockers
rs312481(C;T) is associated with: normal
rs312481(T;T) is associated with: normal

137
-----------
My genotype at rs3774426: TT or (T;T)
rs3774426(C;C) is associated with: better response to certain calcium channel blockers
rs3774426(C;T) is associated with: normal
rs3774426(T;T) is associated with: normal

138
-----------
My genotype at rs358806: CC or (C;C)
rs358806(A;A) is associated with: normal risk of type-2 diabetes
rs358806(A;C) is associated with: 0.9x risk of type-2 diabetes
rs358806(C;C) is associated with: 1.8x risk of type-2 diabetes

139
-----------
My genotype at rs7646054: AA or (A;A)
rs7646054(A;A) is associated with: normal
rs7646054(A;G) is associated with: increased osteoporosis risk
rs7646054(G;G) is associated with: increased osteoporosis risk

140
-----------
My genotype at rs13078807: AA or (A;A)
rs13078807(A;A) is associated with: common, despite what hapmap says

141
-----------
My genotype at rs12487066: TT or (T;T)
rs12487066(C;C) is associated with: >1.09x increased risk for multiple sclerosis
rs12487066(C;T) is associated with: 1.09x increased risk for multiple sclerosis
rs12487066(T;T) is associated with: common

142
-----------
My genotype at rs334558: AA or (A;A)
rs334558(A;A) is associated with: later onset of BP
rs334558(A;G) is associated with: later onset of BP
rs334558(G;G) is associated with: common

143
-----------
My genotype at rs6439886: AA or (A;A)
rs6439886(A;A) is associated with: normal form
rs6439886(A;G) is associated with: ?
rs6439886(G;G) is associated with: increased memory performance

144
-----------
My genotype at rs1803274: CC or (G;G)
rs1803274(A;A) is associated with: possible increased Alzheimer's risk
rs1803274(A;G) is associated with: possible increased Alzheimer's risk
rs1803274(G;G) is associated with: normal

145
-----------
My genotype at rs1799807: TT or (A;A)
rs1799807(A;A) is associated with: Typical BuChE
rs1799807(A;G) is associated with: Heterozygous for "atypical" BuChE
rs1799807(G;G) is associated with: Homozygous for "atypical" BuChE

146
-----------
My genotype at rs2948694: AA or (A;A)
rs2948694(A;A) is associated with: normal
rs2948694(A;G) is associated with: increased risk for heavy alcohol consumption
rs2948694(G;G) is associated with: increased risk for heavy alcohol consumption

147
-----------
My genotype at rs2232165: GG or (C;C)
rs2232165(C;C) is associated with: normal
rs2232165(C;T) is associated with: increased risk for heavy alcohol consumption
rs2232165(T;T) is associated with: increased risk for heavy alcohol consumption

148
-----------
My genotype at rs1131532: AA or (T;T)
rs1131532(C;C) is associated with: normal
rs1131532(C;T) is associated with: normal
rs1131532(T;T) is associated with: 3-6x higher odds of worse outcomes in breast cancer patients

149
-----------
My genotype at rs683395: AA or (T;T)
rs683395(C;C) is associated with: 1.3x risk
rs683395(C;T) is associated with: 1.5x risk
rs683395(T;T) is associated with: normal

150
-----------
My genotype at rs4402960: GG or (G;G)
rs4402960(G;G) is associated with: normal
rs4402960(G;T) is associated with: 1.2x increased risk for type-2 diabetes
rs4402960(T;T) is associated with: 1.2x increased risk for type-2 diabetes

151
-----------
My genotype at rs1470579: AA or (A;A)
rs1470579(A;A) is associated with: normal
rs1470579(A;C) is associated with: 1.2x increased risk for type-2 diabetes
rs1470579(C;C) is associated with: 1.2x increased risk for type-2 diabetes

152
-----------
My genotype at rs2077119: TT or (T;T)
rs2077119(G;G) is associated with: 0.91x decreased risk for T2D
rs2077119(G;T) is associated with: 0.91x decreased risk for T2D
rs2077119(T;T) is associated with: 1x normal risk

153
-----------
My genotype at rs17300539: GG or (G;G)
rs17300539(A;A) is associated with: if obese, dieting more effective
rs17300539(A;G) is associated with: if obese, dieting more effective
rs17300539(G;G) is associated with: normal

154
-----------
My genotype at rs2241766: TT or (T;T)
rs2241766(G;G) is associated with: normal
rs2241766(G;T) is associated with: 0.6x decreased risk for breast cancer
rs2241766(T;T) is associated with: normal

155
-----------
My genotype at rs1501299: GG or (C;C)
rs1501299(A;A) is associated with: normal
rs1501299(A;C) is associated with: normal
rs1501299(C;C) is associated with: 1.8x higher breast cancer risk

156
-----------
My genotype at rs710521: TT or (A;A)
rs710521(A;A) is associated with: 1.4x increased bladder cancer risk
rs710521(A;G) is associated with: 1.2x increased bladder cancer risk
rs710521(G;G) is associated with: normal

157
-----------
My genotype at rs4961: TT or (T;T)
rs4961(G;G) is associated with: normal
rs4961(G;T) is associated with: 1.8x increased risk for high blood pressure
rs4961(T;T) is associated with: 1.8x increased risk for high blood pressure

158
-----------
My genotype at rs8192678: CC or (G;G)
rs8192678(A;A) is associated with: higher blood pressure if <50
rs8192678(A;G) is associated with: higher blood pressure if <50
rs8192678(G;G) is associated with: normal

159
-----------
My genotype at rs8192287: GG or (G;G)
rs8192287(G;G) is associated with: normal
rs8192287(G;T) is associated with: normal
rs8192287(T;T) is associated with: possibly reduced lung function, see details

160
-----------
My genotype at rs8192288: GG or (G;G)
rs8192288(G;G) is associated with: normal
rs8192288(G;T) is associated with: normal
rs8192288(T;T) is associated with: possibly reduced lung function, see details

161
-----------
My genotype at rs35859249: CC or (C;C)
rs35859249(C;C) is associated with: normal
rs35859249(C;T) is associated with: associated with familial obesity
rs35859249(T;T) is associated with: associated with familiar obesity

162
-----------
My genotype at rs4833103: AA or (A;A)
rs4833103(A;A) is associated with: normal
rs4833103(A;C) is associated with: 0.75x decreased risk for Non-hodgkin's lymphoma
rs4833103(C;C) is associated with: 0.74x decreased risk for Non-hodgkin's lymphoma

163
-----------
My genotype at rs1554483: CC or (G;G)
rs1554483(C;C) is associated with: normal
rs1554483(C;G) is associated with: 1.8x higher risk for obesity if in haplotype
rs1554483(G;G) is associated with: 1.8x higher risk for obesity if in haplotype

164
-----------
My genotype at rs4864548: GG or (G;G)
rs4864548(A;A) is associated with: normal
rs4864548(A;G) is associated with: 1.8x higher risk for obesity if in haplotype
rs4864548(G;G) is associated with: 1.8x higher risk for obesity if in haplotype

165
-----------
My genotype at rs629242: CC or (C;C)
rs629242(C;C) is associated with: normal risk
rs629242(C;T) is associated with: somewhat higher risk for prostate cancer
rs629242(T;T) is associated with: somewhat higher risk for prostate cancer

166
-----------
My genotype at rs6836703: GG or (G;G)
rs6836703(A;A) is associated with: 1.34x increased risk for azoospermia in males
rs6836703(A;G) is associated with: 1.34x increased risk for azoospermia in males
rs6836703(G;G) is associated with: normal

167
-----------
My genotype at rs2231142: GG or (C;C)
rs2231142(A;A) is associated with: increased risk of gout; more responsive to rosuvastatin
rs2231142(A;C) is associated with: 1.74x increased gout risk; gefinitib takers 4x more susceptible to diarrhea
rs2231142(C;C) is associated with: normal

168
-----------
My genotype at rs2231137: CC or (G;G)
rs2231137(A;A) is associated with: normal
rs2231137(A;G) is associated with: 2-3x increased risk for ischemic stroke
rs2231137(G;G) is associated with: 2-3x increased risk for ischemic stroke

169
-----------
My genotype at rs356219: AA or (A;A)
rs356219(A;A) is associated with: normal
rs356219(A;G) is associated with: 1.3x increased risk for Parkinson's disease
rs356219(G;G) is associated with: 1.6x increased risk for Parkinson's disease

170
-----------
My genotype at rs2066702: GG or (C;C)
rs2066702(C;C) is associated with: common
rs2066702(C;T) is associated with: None
rs2066702(T;T) is associated with: None

171
-----------
My genotype at rs1573496: CC or (G;G)
rs1573496(C;C) is associated with: normal
rs1573496(C;G) is associated with: 0.68x decreased risk of oral/throat cancers
rs1573496(G;G) is associated with: 0.68x decreased risk of oral/throat cancers

172
-----------
My genotype at rs3816873: TT or (T;T)
rs3816873(C;C) is associated with: reduced risk of type-2 diabetes
rs3816873(C;T) is associated with: None
rs3816873(T;T) is associated with: None

173
-----------
My genotype at rs1585215: TT or (A;A)
rs1585215(A;A) is associated with: normal
rs1585215(A;G) is associated with: 2x increased risk for Hodgkin lymphoma
rs1585215(G;G) is associated with: 3.5x increased risk for Hodgkin lymphoma

174
-----------
My genotype at rs2200733: CC or (C;C)
rs2200733(C;C) is associated with: normal
rs2200733(C;T) is associated with: 1.4x increased risk of atrial fibrillation and ischemic stroke
rs2200733(T;T) is associated with: 1.4x increased risk of atrial fibrillation and ischemic stroke

175
-----------
My genotype at rs10033464: GG or (G;G)
rs10033464(G;G) is associated with: normal
rs10033464(G;T) is associated with: 1.4x increased risk of atrial fibrillation and ischemic stroke
rs10033464(T;T) is associated with: 1.4x increased risk of atrial fibrillation and ischemic stroke

176
-----------
My genotype at rs13149290: CC or (C;C)
rs13149290(C;C) is associated with: somewhat higher risk for prostate cancer
rs13149290(C;T) is associated with: normal risk
rs13149290(T;T) is associated with: normal risk

177
-----------
My genotype at rs3804100: TT or (T;T)
rs3804100(C;C) is associated with: somwhat increased risk for type-1 diabetes and allergic asthma
rs3804100(C;T) is associated with: somewhat increased risk for type-1 diabetes and allergic asthma
rs3804100(T;T) is associated with: normal

178
-----------
My genotype at rs6837793: GG or (G;G)
rs6837793(A;A) is associated with: normal
rs6837793(A;G) is associated with: more likely to gain weight if taking risperidone
rs6837793(G;G) is associated with: more likely to gain weight if taking risperidone

179
-----------
My genotype at rs27072: CC or (C;C)
rs27072(C;C) is associated with: 2x risk of severe alcohol withdrawal
rs27072(C;T) is associated with: normal
rs27072(T;T) is associated with: normal

180
-----------
My genotype at rs27048: CC or (C;C)
rs27048(C;C) is associated with: 2x risk of severe alcohol withdrawal
rs27048(C;T) is associated with: normal
rs27048(T;T) is associated with: normal

181
-----------
My genotype at rs464049: AA or (T;T)
rs464049(C;C) is associated with: decreased risk of schizophrenia in limited study
rs464049(C;T) is associated with: increased risk of schizophrenia in limited study
rs464049(T;T) is associated with: increased risk of schizophrenia in limited study

182
-----------
My genotype at rs1801394: GG or (G;G)
rs1801394(A;A) is associated with: normal
rs1801394(A;G) is associated with: normal
rs1801394(G;G) is associated with: 1.4x higher risk for meningiomas

183
-----------
My genotype at rs10513025: TT or (T;T)
rs10513025(C;C) is associated with: >0.55x reduced risk for autism
rs10513025(C;T) is associated with: 0.55x reduced risk for autism
rs10513025(T;T) is associated with: normal

184
-----------
My genotype at rs16891982: GG or (G;G)
rs16891982(C;C) is associated with: generally non-European, but if European, 7x more likely to have black hair
rs16891982(C;G) is associated with: if European, 7x more likely to have black hair
rs16891982(G;G) is associated with: generally European

185
-----------
My genotype at rs26722: CC or (C;C)
rs26722(C;C) is associated with: normal
rs26722(C;T) is associated with: perhaps darker eye, hair, skin
rs26722(T;T) is associated with: darker eye, hair, skin color

186
-----------
My genotype at rs6897932: CC or (C;C)
rs6897932(C;C) is associated with: 1.5x increased risk for multiple sclerosis
rs6897932(C;T) is associated with: 1.3x increased risk for multiple sclerosis
rs6897932(T;T) is associated with: normal

187
-----------
My genotype at rs3194051: AA or (A;A)
rs3194051(A;A) is associated with: >1.1x risk
rs3194051(A;G) is associated with: 1.12x risk
rs3194051(G;G) is associated with: normal

188
-----------
My genotype at rs17234657: TT or (T;T)
rs17234657(G;G) is associated with: 2.3x risk
rs17234657(G;T) is associated with: 1.5x risk
rs17234657(T;T) is associated with: normal

189
-----------
My genotype at rs889312: CC or (C;C)
rs889312(A;A) is associated with: normal
rs889312(A;C) is associated with: Very slightly higher risk for breast cancer
rs889312(C;C) is associated with: Very slightly higher risk for breast cancer

190
-----------
My genotype at rs966221: GG or (C;C)
rs966221(C;C) is associated with: 1.5x increased stroke risk
rs966221(C;T) is associated with: 1.5x increased stroke risk
rs966221(T;T) is associated with: normal

191
-----------
My genotype at rs17244841: AA or (T;T)
rs17244841(A;A) is associated with: more responsive to statin treatment
rs17244841(A;T) is associated with: not as responsive to statin treatment
rs17244841(T;T) is associated with: not as responsive to statin treatment

192
-----------
My genotype at rs17238540: TT or (T;T)
rs17238540(G;G) is associated with: less responsive to statin treatment
rs17238540(G;T) is associated with: not as responsive to statin treatment
rs17238540(T;T) is associated with: common

193
-----------
My genotype at rs6869366: TT or (T;T)
rs6869366(G;G) is associated with: >2x increased risk for bladder cancer
rs6869366(G;T) is associated with: 2x increased risk for bladder cancer
rs6869366(T;T) is associated with: normal

194
-----------
My genotype at rs6232: TT or (A;A)
rs6232(A;G) is associated with: obesity and insulin
rs6232(G;G) is associated with: obesity and insulin

195
-----------
My genotype at rs27044: CC or (G;G)
rs27044(C;C) is associated with: normal risk
rs27044(C;G) is associated with: 1.4x higher risk for spondylitis
rs27044(G;G) is associated with: 1.4x higher risk for spondylitis

196
-----------
My genotype at rs30187: CC or (C;C)
rs30187(C;C) is associated with: normal risk
rs30187(C;T) is associated with: 1.4x higher risk for spondylitis
rs30187(T;T) is associated with: 1.4x higher risk for spondylitis

197
-----------
My genotype at rs383830: TT or (T;T)
rs383830(A;A) is associated with: 1.9x risk
rs383830(A;T) is associated with: 1.6x risk
rs383830(T;T) is associated with: normal

198
-----------
My genotype at rs27388: GG or (G;G)
rs27388(A;A) is associated with: somewhat increased risk for schizophrenia
rs27388(A;G) is associated with: somewhat increased risk for schizophrenia
rs27388(G;G) is associated with: normal risk

199
-----------
My genotype at rs1355095: TT or (A;A)
rs1355095(A;A) is associated with: normal
rs1355095(A;G) is associated with: None
rs1355095(G;G) is associated with: increase risk of schizophrenia

200
-----------
My genotype at rs6596075: CC or (G;G)
rs6596075(C;C) is associated with: 2x risk
rs6596075(C;G) is associated with: 1.5x risk
rs6596075(G;G) is associated with: normal

201
-----------
My genotype at rs17166496: CC or (G;G)
rs17166496(C;C) is associated with: 1.1x risk
rs17166496(C;G) is associated with: 0.8x risk
rs17166496(G;G) is associated with: normal

202
-----------
My genotype at rs13357391: CC or (C;C)
rs13357391(C;C) is associated with: slightly earlier age at menarche
rs13357391(C;T) is associated with: normal
rs13357391(T;T) is associated with: normal

203
-----------
My genotype at rs1859345: CC or (C;C)
rs1859345(C;C) is associated with: slightly earlier age at menarche
rs1859345(C;T) is associated with: normal
rs1859345(T;T) is associated with: normal

204
-----------
My genotype at rs2303067: AA or (A;A)
rs2303067(A;A) is associated with: 1.8x risk
rs2303067(A;G) is associated with: ?
rs2303067(G;G) is associated with: normal

205
-----------
My genotype at rs1042713: GG or (G;G)
rs1042713(A;A) is associated with: 1.7x increased risk that pediatric inhaler use may make asthma worse
rs1042713(A;G) is associated with: 1.3x increased risk that pediatric inhaler use may make asthma worse
rs1042713(G;G) is associated with: normal

206
-----------
My genotype at rs1042714: GG or (G;G)
rs1042714(C;C) is associated with: normal
rs1042714(C;G) is associated with: complex; see details for increased risks
rs1042714(G;G) is associated with: complex; see details for increased risks

207
-----------
My genotype at rs1800888: CC or (C;C)
rs1800888(C;C) is associated with: normal
rs1800888(C;T) is associated with: increased risk of coronary artery disease
rs1800888(T;T) is associated with: increased risk of coronary artery disease

208
-----------
My genotype at rs13361189: TT or (T;T)
rs13361189(C;C) is associated with: 2.6x increased risk for Crohn's disease
rs13361189(C;T) is associated with: 1.3x increased risk for Crohn's disease
rs13361189(T;T) is associated with: normal

209
-----------
My genotype at rs4958847: GG or (G;G)
rs4958847(A;A) is associated with: 2.6x increased risk for Crohn's disease
rs4958847(A;G) is associated with: 1.3x increased risk for Crohn's disease
rs4958847(G;G) is associated with: normal

210
-----------
My genotype at rs1000113: CC or (C;C)
rs1000113(C;C) is associated with: normal
rs1000113(C;T) is associated with: 1.5x risk of Crohn's disease
rs1000113(T;T) is associated with: 1.9x risk of Crohn's disease

211
-----------
My genotype at rs3212227: TT or (A;A)
rs3212227(A;A) is associated with: 1.4x increased risk of psoriasis and psoriatic arthritis
rs3212227(A;C) is associated with: None
rs3212227(C;C) is associated with: normal

212
-----------
My genotype at rs6887695: GG or (G;G)
rs6887695(C;C) is associated with: normal
rs6887695(C;G) is associated with: 
rs6887695(G;G) is associated with: 1.4x increased risk of psoriasis, psoriatic arthritis

213
-----------
My genotype at rs2910164: GG or (G;G)
rs2910164(C;C) is associated with: higher/earlier cancer likelihood??
rs2910164(C;G) is associated with: higher/earlier cancer likelihood??
rs2910164(G;G) is associated with: normal

214
-----------
My genotype at rs3095870: CC or (G;G)
rs3095870(A;A) is associated with: normal risk
rs3095870(A;G) is associated with: 1.7x increased risk for SLE (lupus)
rs3095870(G;G) is associated with: 1.7x increased risk for SLE (lupus)

215
-----------
My genotype at rs872071: AA or (A;A)
rs872071(A;A) is associated with: normal
rs872071(A;G) is associated with: ~1.5x increased risk for chronic lymphocytic leukemia
rs872071(G;G) is associated with: ~1.5x increased risk for chronic lymphocytic leukemia

216
-----------
My genotype at rs1334710: AA or (A;A)
rs1334710(A;A) is associated with: average
rs1334710(A;G) is associated with: increased risk
rs1334710(G;G) is associated with: increased risk

217
-----------
My genotype at rs1018381: GG or (C;C)
rs1018381(T;T) is associated with: impaired cognitive ability

218
-----------
My genotype at rs1142345: TT or (A;A)
rs1142345(G;G) is associated with: possibly incapable of detoxifying

219
-----------
My genotype at rs1800584: CC or (G;G)
rs1800584(A;A) is associated with: TPMT*4A homozygote; likely issues detoxifying certain drugs
rs1800584(A;G) is associated with: TPMT*4A heterozygote; possible issues detoxifying certain drugs

220
-----------
My genotype at rs1800460: CC or (G;G)
rs1800460(A;A) is associated with: incapable of detoxifying byproducts of certain drugs
rs1800460(A;G) is associated with: normal
rs1800460(G;G) is associated with: normal

221
-----------
My genotype at rs1800462: CC or (G;G)
rs1800462(C;C) is associated with: incapable of detoxifying
rs1800462(C;G) is associated with: detoxifying ability may be diminished
rs1800462(G;G) is associated with: normal for 23andMe

222
-----------
My genotype at rs7754840: CC or (G;G)
rs7754840(C;C) is associated with: 1.3x increased risk for type-2 diabetes
rs7754840(C;G) is associated with: 1.3x increased risk for type-2 diabetes
rs7754840(G;G) is associated with: normal

223
-----------
My genotype at rs793862: GG or (G;G)
rs793862(A;A) is associated with: 3-5x dyslexia risk
rs793862(A;G) is associated with: increased dyslexia risk
rs793862(G;G) is associated with: common

224
-----------
My genotype at rs807701: AA or (T;T)
rs807701(C;C) is associated with: 2-5x increased dyslexia risk
rs807701(C;T) is associated with: increased dyslexia risk
rs807701(T;T) is associated with: common

225
-----------
My genotype at rs4504469: CC or (C;C)
rs4504469(C;C) is associated with: common
rs4504469(C;T) is associated with: 1.5x risk
rs4504469(T;T) is associated with: > 1.5x risk

226
-----------
My genotype at rs761100: CC or (G;G)
rs761100(G;G) is associated with: higher risk for dyslexia
rs761100(G;T) is associated with: normal risk
rs761100(T;T) is associated with: normal risk

227
-----------
My genotype at rs3212236: TT or (A;A)
rs3212236(A;A) is associated with: higher risk for dyslexia
rs3212236(A;G) is associated with: normal risk
rs3212236(G;G) is associated with: normal risk

228
-----------
My genotype at rs2143340: AA or (T;T)
rs2143340(C;C) is associated with: > 2x risk of dyslexia and poor reading performance
rs2143340(C;T) is associated with: increased risk of dyslexia and poor reading performance
rs2143340(T;T) is associated with: common

229
-----------
My genotype at rs1799945: CC or (G;G)
rs1799945(C;C) is associated with: Not a H63D hemochromatosis carrier.
rs1799945(C;G) is associated with: One copy of H63D, carrier of hemochromatosis, likely unaffected unless also C282Y carrier.
rs1799945(G;G) is associated with: Two copies of H36D, likely affected by mild form of hemochromatosis

230
-----------
My genotype at rs1800562: GG or (G;G)
rs1800562(A;A) is associated with: Two copies of H36D, likely affected by hemochromatosis which may be serious if male or post-menopausal.
rs1800562(A;G) is associated with: One copy of C282Y, carrier of hemochromatosis, likely unaffected unless also H63D carrier.
rs1800562(G;G) is associated with: Not a C282Y hemochromatosis carrier.

231
-----------
My genotype at rs4959039: AA or (A;A)
rs4959039(A;A) is associated with: normal
rs4959039(A;G) is associated with: 1.4x higher risk for multiple sclerosis
rs4959039(G;G) is associated with: 1.6x higher risk for multiple sclerosis

232
-----------
My genotype at rs1265159: GG or (C;C)
rs1265159(C;C) is associated with: normal
rs1265159(C;T) is associated with: ~5x increased risk of psoriasis
rs1265159(T;T) is associated with: psoriasis risk for Chinese?

233
-----------
My genotype at rs1265181: GG or (G;G)
rs1265181(C;C) is associated with: normal
rs1265181(C;G) is associated with: increased risk for psoriasis
rs1265181(G;G) is associated with: possibly increased risk of psoriasis

234
-----------
My genotype at rs2395029: TT or (T;T)
rs2395029(G;G) is associated with: HLA-B*5701 homozygote; high risk for hypersensitivity to various drugs including abacavir; see details
rs2395029(G;T) is associated with: HLA-B*5701 carrier
rs2395029(T;T) is associated with: common

235
-----------
My genotype at rs1800630: CC or (C;C)
rs1800630(A;A) is associated with: 1.8x increased lupus risk
rs1800630(A;C) is associated with: 1.8x increased lupus risk
rs1800630(C;C) is associated with: normal

236
-----------
My genotype at rs1800750: GG or (G;G)
rs1800750(A;A) is associated with: higher acute otitis risk
rs1800750(A;G) is associated with: normal risk
rs1800750(G;G) is associated with: normal risk

237
-----------
My genotype at rs361525: GG or (G;G)
rs361525(A;A) is associated with: complex; generally higher risk for certain diseases
rs361525(A;G) is associated with: complex; generally higher risk for certain diseases
rs361525(G;G) is associated with: complex; generally normal risk

238
-----------
My genotype at rs9332739: GG or (G;G)
rs9332739(C;C) is associated with: reduced risk of age related macular degeneration
rs9332739(C;G) is associated with: None
rs9332739(G;G) is associated with: normal

239
-----------
My genotype at rs419788: CC or (G;G)
rs419788(A;A) is associated with: 2.3x risk for lupus
rs419788(A;G) is associated with: 2.0x risk for lupus
rs419788(G;G) is associated with: average

240
-----------
My genotype at rs2070600: CC or (G;G)
rs2070600(A;A) is associated with: 1.5x increased risk for gastric cancer
rs2070600(A;G) is associated with: 1.5x increased risk for gastric cancer
rs2070600(G;G) is associated with: normal

241
-----------
My genotype at rs3131296: CC or (G;G)
rs3131296(A;A) is associated with: normal
rs3131296(A;G) is associated with: 1.2x increased risk for schizophrenia
rs3131296(G;G) is associated with: 1.4x increased risk for schizophrenia

242
-----------
My genotype at rs6910071: AA or (A;A)
rs6910071(A;A) is associated with: normal
rs6910071(A;G) is associated with: possibly at 4x higher risk of [[rheumatoid arthritis]]
rs6910071(G;G) is associated with: 6x higher risk of [[rheumatoid arthritis]]

243
-----------
My genotype at rs3129934: CC or (C;C)
rs3129934(C;C) is associated with: normal
rs3129934(C;T) is associated with: normal
rs3129934(T;T) is associated with: 3.3x increased risk for multiple sclerosis

244
-----------
My genotype at rs3817964: TT or (T;T)
rs3817964(A;A) is associated with: normal
rs3817964(A;T) is associated with: possibly at 4x higher risk of [[rheumatoid arthritis]]
rs3817964(T;T) is associated with: 6x higher risk of [[rheumatoid arthritis]]

245
-----------
My genotype at rs10947262: CC or (C;C)
rs10947262(C;C) is associated with: 1.3x increased risk for osteoarthritis

246
-----------
My genotype at rs3135391: GG or (C;C)
rs3135391(C;C) is associated with: normal
rs3135391(C;T) is associated with: HLA-DRB1*1501 carrier; higher multiple sclerosis risk
rs3135391(T;T) is associated with: 3 to 6 fold higher risk for multiple sclerosis

247
-----------
My genotype at rs3135388: GG or (C;C)
rs3135388(C;C) is associated with: normal
rs3135388(C;T) is associated with: 3x higher risk of multiple sclerosis
rs3135388(T;T) is associated with: 3-6x higher risk of multiple sclerosis

248
-----------
My genotype at rs660895: AA or (A;A)
rs660895(A;A) is associated with: normal
rs660895(A;G) is associated with: possibly at 4x higher risk of [[rheumatoid arthritis]]
rs660895(G;G) is associated with: 6x higher risk of rheumatoid arthritis

249
-----------
My genotype at rs9272346: GG or (G;G)
rs9272346(A;A) is associated with: 18.5x risk of Type-1 Diabetes
rs9272346(A;G) is associated with: 5.5x risk type-1 diabetes
rs9272346(G;G) is associated with: normal

250
-----------
My genotype at rs2187668: CC or (G;G)
rs2187668(A;A) is associated with: Autoimmune disorder risk (lupus, celiac disease) due to 2 HLA-DRB1*0301 alleles
rs2187668(A;G) is associated with: Somewhat increased autoimmune disorder (lupus, celiac disease) risk; 1 HLA-DRB1*0301 allele
rs2187668(G;G) is associated with: average

251
-----------
My genotype at rs9469220: AA or (A;A)
rs9469220(A;A) is associated with: 1.5x risk
rs9469220(A;G) is associated with: 1.1x risk
rs9469220(G;G) is associated with: normal

252
-----------
My genotype at rs6457617: TT or (T;T)
rs6457617(C;C) is associated with: normal
rs6457617(C;T) is associated with: 2.3x risk of rheumatoid arthritis
rs6457617(T;T) is associated with: 5.2x risk of rheumatoid arthritis

253
-----------
My genotype at rs7454108: TT or (T;T)
rs7454108(C;C) is associated with: Homozygous for HLA-DQ8 haplotype
rs7454108(C;T) is associated with: Single HLA-DQ8 haplotype

254
-----------
My genotype at rs241448: AA or (T;T)
rs241448(C;C) is associated with: 2.14x increased risk for Alzheimer's
rs241448(C;T) is associated with: 1.51x increased risk for Alzheimer's
rs241448(T;T) is associated with: common

255
-----------
My genotype at rs1800454: CC or (G;G)
rs1800454(A;A) is associated with: affected
rs1800454(A;G) is associated with: carrier
rs1800454(G;G) is associated with: normal

256
-----------
My genotype at rs7757037: AA or (A;A)
rs7757037(A;A) is associated with: 0.63x decreased risk for bipolar disorder
rs7757037(A;G) is associated with: 0.68x decreased risk for bipolar disorder
rs7757037(G;G) is associated with: normal

257
-----------
My genotype at rs1360780: CC or (C;C)
rs1360780(C;C) is associated with: normal
rs1360780(C;T) is associated with: 1.3x increased risk for depression
rs1360780(T;T) is associated with: 1.3x increased risk for depression

258
-----------
My genotype at rs1801270: CC or (C;C)
rs1801270(A;A) is associated with: increased risk for lung cancer
rs1801270(A;C) is associated with: increased risk for lung cancer
rs1801270(C;C) is associated with: normal risk

259
-----------
My genotype at rs4714156: CC or (C;C)
rs4714156(C;C) is associated with: <0.61x risk for restless legs
rs4714156(C;T) is associated with: 0.61x risk for restless legs
rs4714156(T;T) is associated with: common

260
-----------
My genotype at rs9296249: TT or (T;T)
rs9296249(C;C) is associated with: <0.62x risk for restless legs
rs9296249(C;T) is associated with: 0.62x risk for restless legs
rs9296249(T;T) is associated with: common

261
-----------
My genotype at rs9357271: TT or (T;T)
rs9357271(C;C) is associated with: <0.63x risk for restless legs
rs9357271(C;T) is associated with: 0.63x risk for restless legs
rs9357271(T;T) is associated with: common

262
-----------
My genotype at rs3923809: AA or (A;A)
rs3923809(A;A) is associated with: >1.9x risk for restless legs
rs3923809(A;G) is associated with: 1.9x risk for restless legs
rs3923809(G;G) is associated with: common

263
-----------
My genotype at rs6458307: TT or (T;T)
rs6458307(C;C) is associated with: 1.4x risk
rs6458307(C;T) is associated with: 0.8x risk
rs6458307(T;T) is associated with: normal

264
-----------
My genotype at rs699947: CC or (C;C)
rs699947(A;A) is associated with: 1.36x increased risk for thyroid cancer in men
rs699947(A;C) is associated with: 1.36x increased risk for thyroid cancer in men
rs699947(C;C) is associated with: normal

265
-----------
My genotype at rs1570360: GG or (G;G)
rs1570360(A;A) is associated with: 3x risk
rs1570360(A;G) is associated with: 3x risk
rs1570360(G;G) is associated with: normal

266
-----------
My genotype at rs3025039: CC or (C;C)
rs3025039(C;C) is associated with: normal
rs3025039(C;T) is associated with: 2.6x increased risk for ARMD
rs3025039(T;T) is associated with: 2.6x increased risk for ARMD

267
-----------
My genotype at rs7771980: TT or (T;T)
rs7771980(C;C) is associated with: lower bone mineral density in postmenopausal Korean women
rs7771980(C;T) is associated with: higher bone mineral density in postmenopausal Spanish women
rs7771980(T;T) is associated with: normal

268
-----------
My genotype at rs2275913: AA or (A;A)
rs2275913(A;A) is associated with: 3x increased gastric cancer risk
rs2275913(A;G) is associated with: 1.4x increased gastric cancer risk
rs2275913(G;G) is associated with: normal

269
-----------
My genotype at rs3804505: GG or (C;C)
rs3804505(C;T) is associated with: ?
rs3804505(T;T) is associated with: rare, related to myoclonic epilepsy

270
-----------
My genotype at rs2653349: GG or (G;G)
rs2653349(A;A) is associated with: normal
rs2653349(A;G) is associated with: ~1.5x? increased risk for cluster headaches
rs2653349(G;G) is associated with: 2-6x increased risk for cluster headaches

271
-----------
My genotype at rs2518224: AA or (A;A)
rs2518224(A;A) is associated with: normal
rs2518224(A;C) is associated with: normal
rs2518224(C;C) is associated with: 8.2x higher risk of suicidal thoughts when taking [[citalopram]]

272
-----------
My genotype at rs619203: GG or (G;G)
rs619203(C;C) is associated with: 
rs619203(C;G) is associated with: increases susceptibility to Myocardial Infarction 1.15 times
rs619203(G;G) is associated with: None

273
-----------
My genotype at rs6918698: GG or (G;G)
rs6918698(C;C) is associated with: normal risk
rs6918698(C;G) is associated with: ~normal risk
rs6918698(G;G) is associated with: 2.2x higher systemic sclerosis risk

274
-----------
My genotype at rs6920220: GG or (G;G)
rs6920220(A;A) is associated with: 1.7x risk
rs6920220(A;G) is associated with: 1.2x risk
rs6920220(G;G) is associated with: normal

275
-----------
My genotype at rs7753394: TT or (T;T)
rs7753394(C;C) is associated with: 1.5x risk
rs7753394(C;T) is associated with: 1.2x risk
rs7753394(T;T) is associated with: normal

276
-----------
My genotype at rs237025: GG or (C;C)
rs237025(C;C) is associated with: VAL/VAL reduced [[diabetes]] susceptibility
rs237025(C;T) is associated with: contributes to both type-1 diabetes and type-2 diabetes
rs237025(T;T) is associated with: MET/MET increased diabetes susceptibility

277
-----------
My genotype at rs6922269: GG or (G;G)
rs6922269(A;A) is associated with: 1.6x risk
rs6922269(A;G) is associated with: 1.2x risk
rs6922269(G;G) is associated with: normal

278
-----------
My genotype at rs2881766: TT or (T;T)
rs2881766(G;G) is associated with: normal
rs2881766(G;T) is associated with: increased risk for pregnancy-induced hypertension
rs2881766(T;T) is associated with: increased risk for pregnancy-induced hypertension

279
-----------
My genotype at rs3020314: TT or (T;T)
rs3020314(C;C) is associated with: 0.42x reduced lymphoma risk
rs3020314(C;T) is associated with: 0.64x reduced lymphoma risk
rs3020314(T;T) is associated with: normal

280
-----------
My genotype at rs2179922: GG or (G;G)
rs2179922(A;A) is associated with: males 1-2cm shorter on average
rs2179922(G;G) is associated with: common

281
-----------
My genotype at rs2295190: GG or (G;G)
rs2295190(G;G) is associated with: common
rs2295190(G;T) is associated with: Slightly increased risk for ovarian cancer in women
rs2295190(T;T) is associated with: Slightly increased risk for ovarian cancer in women

282
-----------
My genotype at rs1799971: AA or (A;A)
rs1799971(A;A) is associated with: normal
rs1799971(A;G) is associated with: stronger cravings for alcohol. if alcoholic, naltrexone treatment 2x more successful
rs1799971(G;G) is associated with: more pain

283
-----------
My genotype at rs10485057: AA or (A;A)
rs10485057(A;A) is associated with: normal
rs10485057(A;G) is associated with: normal?
rs10485057(G;G) is associated with: increased risk for smoking, nicotine dependence

284
-----------
My genotype at rs622342: CC or (C;C)
rs622342(C;C) is associated with: influences dosage for Parkinson's patients

285
-----------
My genotype at rs3798220: TT or (T;T)
rs3798220(C;C) is associated with: 2-3x higher risk for cardiovascular events, which can be lowered by aspirin
rs3798220(C;T) is associated with: 2-3x higher risk for cardiovascular events, which can be lowered by aspirin
rs3798220(T;T) is associated with: normal

286
-----------
My genotype at rs10455872: AA or (A;A)
rs10455872(A;G) is associated with: increased Coronary Heart disease risk
rs10455872(G;G) is associated with: increased Coronary Heart disease risk

287
-----------
My genotype at rs992037: CC or (C;C)
rs992037(C;C) is associated with: lowest lysine values
rs992037(C;T) is associated with: intermediate lysine values
rs992037(T;T) is associated with: highest lysine values

288
-----------
My genotype at rs13208776: GG or (G;G)
rs13208776(A;A) is associated with: normal
rs13208776(A;G) is associated with: normal
rs13208776(G;G) is associated with: higher risk for generalized vitiligo

289
-----------
My genotype at rs8089: CC or (G;G)
rs8089(G;G) is associated with: slightly increased heart attack risk
rs8089(G;T) is associated with: slightly increased heart attack risk
rs8089(T;T) is associated with: normal risk

290
-----------
My genotype at rs1800795: CC or (G;G)
rs1800795(C;C) is associated with: less IL6; certain risks, see details
rs1800795(C;G) is associated with: complex; see details
rs1800795(G;G) is associated with: more IL6; certain risks, see details

291
-----------
My genotype at rs10250779: CC or (C;C)
rs10250779(C;C) is associated with: normal
rs10250779(C;T) is associated with: normal
rs10250779(T;T) is associated with: possible exercise-inducing cramping in African-Americans

292
-----------
My genotype at rs2302009: AA or (T;T)
rs2302009(G;G) is associated with: 4.6x risk
rs2302009(G;T) is associated with: normal
rs2302009(T;T) is associated with: normal

293
-----------
My genotype at rs1057868: CC or (C;C)
rs1057868(C;C) is associated with: normal
rs1057868(C;T) is associated with: normal
rs1057868(T;T) is associated with: 1.6x higher overall CYP3A activity

294
-----------
My genotype at rs1334512: GG or (G;G)
rs1334512(G;G) is associated with: 0.37x decreased risk for severe malaria
rs1334512(G;T) is associated with: decreased risk for severe malaria
rs1334512(T;T) is associated with: normal

295
-----------
My genotype at rs12536657: GG or (G;G)
rs12536657(A;A) is associated with: hypermyopia risk

296
-----------
My genotype at rs1128503: GG or (C;C)
rs1128503(C;C) is associated with: normal
rs1128503(C;T) is associated with: may require more methadone during heroin withdrawal
rs1128503(T;T) is associated with: likely to require more methadone during heroin withdrawal

297
-----------
My genotype at rs662: TT or (A;A)
rs662(A;A) is associated with: 0.65x lower risk of ovarian cancer; normal PON catalytic efficiency
rs662(A;G) is associated with: 0.65x lower risk of ovarian cancer; higher risk of coronary heart disease in some studies; somewhat reduced PON catalytic efficiency
rs662(G;G) is associated with: higher risk of coronary heart disease in some studies; significantly reduced PON catalytic efficiency; increased trait-anxiety scores

298
-----------
My genotype at rs705381: CC or (C;C)
rs705381(C;C) is associated with: normal
rs705381(C;T) is associated with: less likely to gain weight if taking risperidone
rs705381(T;T) is associated with: less likely to gain weight if taking risperidone

299
-----------
My genotype at rs41279854: AA or (A;A)
rs41279854(G;G) is associated with: CYP3A5*10 homozygote; nonexpressor for CYP3A5
rs41279854(A;G) is associated with: carrier of one CYP3A5*10 allele
rs41279854(A;A) is associated with: normal

300
-----------
My genotype at rs28365083: GG or (C;C)
rs28365083(A;A) is associated with: CYP3A5*2 homozygote; nonexpressor for CYP3A5
rs28365083(A;C) is associated with: carrier of one CYP3A5*2 allele
rs28365083(C;C) is associated with: normal

301
-----------
My genotype at rs28383479: CC or (G;G)
rs28383479(A;A) is associated with: CYP3A5*9 homozygote; nonexpressor for CYP3A5
rs28383479(A;G) is associated with: carrier of one CYP3A5*9 allele
rs28383479(G;G) is associated with: normal

302
-----------
My genotype at rs10264272: CC or (C;C)
rs10264272(C;C) is associated with: normal
rs10264272(C;T) is associated with: carrier of one CYP3A5*6 allele
rs10264272(T;T) is associated with: CYP3A5*6 homozygote; nonexpressor for CYP3A5

303
-----------
My genotype at rs56411402: TT or (T;T)
rs56411402(C;C) is associated with: CYP3A5*4 homozygote; nonexpressor for CYP3A5
rs56411402(C;T) is associated with: carrier of one CYP3A5*4 allele
rs56411402(T;T) is associated with: normal

304
-----------
My genotype at rs41279857: GG or (G;G)
rs41279857(T;T) is associated with: CYP3A5*S100Y homozygote; nonexpressor for CYP3A5
rs41279857(G;T) is associated with: carrier of one CYP3A5*S100Y allele
rs41279857(G;G) is associated with: normal

305
-----------
My genotype at rs56244447: AA or (A;A)
rs56244447(A;A) is associated with: normal
rs56244447(A;C) is associated with: carrier of one CYP3A5*3D allele
rs56244447(C;C) is associated with: CYP3A5*3D homozygote; nonexpressor for CYP3A5

306
-----------
My genotype at rs776746: CC or (G;G)
rs776746(A;A) is associated with: nonfunctional CYP3A5; drug metabolism effects
rs776746(A;G) is associated with: carrier of 1 nonfunctional CYP3A5 allele; drug metabolism affects

307
-----------
My genotype at rs72552791: TT or (A;A)
rs72552791(G;G) is associated with: CYP3A5*11 homozygote; nonexpressor for CYP3A5
rs72552791(A;G) is associated with: carrier of one CYP3A5*11 allele
rs72552791(A;A) is associated with: normal

308
-----------
My genotype at rs28383468: GG or (C;C)
rs28383468(C;C) is associated with: normal
rs28383468(C;T) is associated with: carrier of one CYP3A5*H30Y allele
rs28383468(T;T) is associated with: CYP3A5*H30Y homozygote; nonexpressor for CYP3A5

309
-----------
My genotype at rs55817950: GG or (G;G)
rs55817950(A;A) is associated with: CYP3A5*8 homozygote; nonexpressor for CYP3A5
rs55817950(A;G) is associated with: carrier of one CYP3A5*8 allele
rs55817950(G;G) is associated with: normal

310
-----------
My genotype at rs4986913: GG or (C;C)
rs4986913(C;C) is associated with: normal
rs4986913(C;T) is associated with: carrier of one CYP3A4*19 allele
rs4986913(T;T) is associated with: CYP3A4*19 homozygote

311
-----------
My genotype at rs4986910: AA or (T;T)
rs4986910(C;C) is associated with: CYP3A4*3 homozygote
rs4986910(C;T) is associated with: carrier of one CYP3A4*3 allele
rs4986910(T;T) is associated with: normal

312
-----------
My genotype at rs1041988: AA or (T;T)
rs1041988(C;C) is associated with: CYP3A4*_23139T>C(I431T) homozygote
rs1041988(C;T) is associated with: carrier of one CYP3A4*_23139T>C(I431T) allele
rs1041988(T;T) is associated with: normal

313
-----------
My genotype at rs4986909: GG or (C;C)
rs4986909(C;C) is associated with: normal
rs4986909(C;T) is associated with: carrier of one CYP3A4*13 allele
rs4986909(T;T) is associated with: CYP3A4*13 homozygote

314
-----------
My genotype at rs67784355: GG or (G;G)
rs67784355(A;A) is associated with: CYP3A4*11 homozygote
rs67784355(A;G) is associated with: carrier of one CYP3A4*11 allele
rs67784355(G;G) is associated with: normal

315
-----------
My genotype at rs28371759: AA or (T;T)
rs28371759(C;C) is associated with: CYP3A4*18 homozygote
rs28371759(C;T) is associated with: carrier of one CYP3A4*18 allele
rs28371759(T;T) is associated with: normal

316
-----------
My genotype at rs3208363: AA or (T;T)
rs3208363(G;G) is associated with: CYP3A4*_16907T>G(S252A) homozygote
rs3208363(G;T) is associated with: carrier of one CYP3A4*_16907T>G(S252A) allele
rs3208363(T;T) is associated with: normal

317
-----------
My genotype at rs55785340: AA or (A;A)
rs55785340(G;G) is associated with: CYP3A4*2 homozygote
rs55785340(A;G) is associated with: carrier of one CYP3A4*2 allele
rs55785340(A;A) is associated with: normal

318
-----------
My genotype at rs55901263: GG or (G;G)
rs55901263(C;C) is associated with: CYP3A4*5 homozygote
rs55901263(C;G) is associated with: carrier of one CYP3A4*5 allele
rs55901263(G;G) is associated with: normal

319
-----------
My genotype at rs3208361: TT or (A;A)
rs3208361(A;A) is associated with: normal
rs3208361(A;G) is associated with: carrier of one CYP3A4*_15635A>G(I193V) allele
rs3208361(G;G) is associated with: CYP3A4*_15635A>G(I193V)  homozygote

320
-----------
My genotype at rs4987161: AA or (T;T)
rs4987161(C;C) is associated with: CYP3A4*17 homozygote
rs4987161(C;T) is associated with: carrier of one CYP3A4*17 allele
rs4987161(T;T) is associated with: normal

321
-----------
My genotype at rs12721627: GG or (G;G)
rs12721627(C;C) is associated with: normal
rs12721627(C;G) is associated with: carrier of one CYP3A4*16 allele
rs12721627(G;G) is associated with: CYP3A4*16 homozygote

322
-----------
My genotype at rs4986908: CC or (G;G)
rs4986908(A;A) is associated with: CYP3A4*_14313G>A(E174H) homozygote
rs4986908(A;G) is associated with: carrier of one CYP3A4*_14313G>A(E174H) allele
rs4986908(G;G) is associated with: normal

323
-----------
My genotype at rs4986907: CC or (G;G)
rs4986907(A;A) is associated with: CYP3A4*15A homozygote
rs4986907(A;G) is associated with: carrier of one CYP3A4*15A allele
rs4986907(G;G) is associated with: normal

324
-----------
My genotype at rs55951658: TT or (T;T)
rs55951658(C;C) is associated with: CYP3A4*4 homozygote
rs55951658(C;T) is associated with: carrier of one CYP3A4*4 allele
rs55951658(T;T) is associated with: normal

325
-----------
My genotype at rs3091339: TT or (A;A)
rs3091339(A;A) is associated with: normal
rs3091339(A;G) is associated with: carrier of one CYP3A4*_11460A>G(K96E) allele
rs3091339(G;G) is associated with: CYP3A4*_11460A>G(K96E) homozygote

326
-----------
My genotype at rs56324128: CC or (C;C)
rs56324128(C;C) is associated with: normal
rs56324128(C;T) is associated with: carrier of one CYP3A4*7 allele
rs56324128(T;T) is associated with: CYP3A4*7 homozygote

327
-----------
My genotype at rs12721634: AA or (T;T)
rs12721634(C;C) is associated with: CYP3A4*14 homozygote
rs12721634(C;T) is associated with: carrier of one CYP3A4*14 allele
rs12721634(T;T) is associated with: normal

328
-----------
My genotype at rs2740574: TT or (A;A)
rs2740574(A;A) is associated with: normal
rs2740574(A;G) is associated with: carrier of one CYP3A4*1B allele
rs2740574(G;G) is associated with: 2.5x increased risk for prostate or ovarian cancer; CYP3A4*1B homozygote

329
-----------
My genotype at rs2227692: CC or (C;C)
rs2227692(C;T) is associated with: 1.6x higher risk for diffuse gastric cancer
rs2227692(T;T) is associated with: 1.6x higher risk for diffuse gastric cancer

330
-----------
My genotype at rs7341475: GG or (G;G)
rs7341475(A;A) is associated with: normal
rs7341475(A;G) is associated with: normal
rs7341475(G;G) is associated with: 1.58x increased schizophrenia risk for women

331
-----------
My genotype at rs1799999: CC or (G;G)
rs1799999(G;G) is associated with: normal risk
rs1799999(G;T) is associated with: 
rs1799999(T;T) is associated with: insulin resistance

332
-----------
My genotype at rs4730751: CC or (C;C)
rs4730751(A;A) is associated with: For kidney donors, 2x more likely to result in allograft rejection

333
-----------
My genotype at rs1858830: CC or (G;G)
rs1858830(C;C) is associated with: 2x risk of autism
rs1858830(C;G) is associated with: 1.6x increased autism risk
rs1858830(G;G) is associated with: normal

334
-----------
My genotype at rs213950: GG or (G;G)
rs213950(A;A) is associated with: >1.1x risk
rs213950(A;G) is associated with: 1.1x risk
rs213950(G;G) is associated with: normal

335
-----------
My genotype at rs11761231: CC or (C;C)
rs11761231(C;C) is associated with: 
rs11761231(C;T) is associated with: 
rs11761231(T;T) is associated with: normal

336
-----------
My genotype at rs3807153: AA or (T;T)
rs3807153(C;C) is associated with: Distal Renal Tubular Acidosis
rs3807153(C;T) is associated with: carrier
rs3807153(T;T) is associated with: normal

337
-----------
My genotype at rs10246939: TT or (T;T)
rs10246939(C;C) is associated with: can taste bitter
rs10246939(C;T) is associated with: can taste bitter
rs10246939(T;T) is associated with: possibly unable to taste bitterness

338
-----------
My genotype at rs1726866: AA or (T;T)
rs1726866(C;C) is associated with: can taste bitter
rs1726866(C;T) is associated with: can taste bitter
rs1726866(T;T) is associated with: possible unable to taste bitter

339
-----------
My genotype at rs713598: CC or (G;G)
rs713598(C;C) is associated with: can taste bitter
rs713598(C;G) is associated with: can taste bitter
rs713598(G;G) is associated with: possibly unable to taste bitter

340
-----------
My genotype at rs8176058: GG or (C;C)
rs8176058(C;C) is associated with: common
rs8176058(C;T) is associated with: None
rs8176058(T;T) is associated with: None

341
-----------
My genotype at rs7794745: AA or (T;T)
rs7794745(A;A) is associated with: normal risk
rs7794745(A;T) is associated with: slightly increased risk for autism
rs7794745(T;T) is associated with: slightly increased risk for autism

342
-----------
My genotype at rs851715: TT or (A;A)
rs851715(A;A) is associated with: risk of speech development delay and/or impairment
rs851715(A;G) is associated with: None
rs851715(G;G) is associated with: None

343
-----------
My genotype at rs10246256: TT or (T;T)
rs10246256(C;C) is associated with: None
rs10246256(C;T) is associated with: None
rs10246256(T;T) is associated with: higher risk of speech development delay and/or impairment

344
-----------
My genotype at rs2710102: GG or (C;C)
rs2710102(C;C) is associated with: higher risk of speech development delay and/or impairment
rs2710102(C;T) is associated with: None
rs2710102(T;T) is associated with: None

345
-----------
My genotype at rs759178: CC or (G;G)
rs759178(G;G) is associated with: higher risk of speech development delay and/or impairment
rs759178(G;T) is associated with: None
rs759178(T;T) is associated with: None

346
-----------
My genotype at rs1922892: TT or (T;T)
rs1922892(C;C) is associated with: None
rs1922892(C;T) is associated with: None
rs1922892(T;T) is associated with: higher risk of speech development delay and/or impairment

347
-----------
My genotype at rs2538991: CC or (G;G)
rs2538991(G;G) is associated with: higher risk of speech development delay and/or impairment
rs2538991(G;T) is associated with: None
rs2538991(T;T) is associated with: None

348
-----------
My genotype at rs2538976: CC or (G;G)
rs2538976(A;A) is associated with: None
rs2538976(A;G) is associated with: None
rs2538976(G;G) is associated with: higher risk for speech development delay and/or impairment

349
-----------
My genotype at rs2710117: AA or (T;T)
rs2710117(A;A) is associated with: higher risk of speech development delay and/or impairment
rs2710117(A;T) is associated with: None
rs2710117(T;T) is associated with: None

350
-----------
My genotype at rs17173608: TT or (T;T)
rs17173608(G;G) is associated with: lower visceral adipose tissue
rs17173608(G;T) is associated with: lower visceral adipose tissue
rs17173608(T;T) is associated with: normal

351
-----------
My genotype at rs3218536: CC or (G;G)
rs3218536(A;A) is associated with: lower risk for breast, ovarian cancer
rs3218536(A;G) is associated with: lower risk for breast, ovarian cancer
rs3218536(G;G) is associated with: normal risk

352
-----------
My genotype at rs10239794: CC or (C;C)
rs10239794(C;C) is associated with: average
rs10239794(C;T) is associated with: 1.3x risk for ALS
rs10239794(T;T) is associated with: >1.3x risk for ALS

353
-----------
My genotype at rs10260404: CC or (C;C)
rs10260404(C;C) is associated with: 1.6x risk for ALS
rs10260404(C;T) is associated with: 1.2x risk for ALS
rs10260404(T;T) is associated with: average

354
-----------
My genotype at rs2515475: CC or (C;C)
rs2515475(C;C) is associated with: normal
rs2515475(C;T) is associated with: 1.27x increased ARDS risk in critically ill patients
rs2515475(T;T) is associated with: 1.27x increased ARDS risk in critically ill patients

355
-----------
My genotype at rs268: AA or (A;A)
rs268(A;G) is associated with: 3X increased risk for venous thromboembolism
rs268(G;G) is associated with: 3X+ increased risk for venous thromboembolism

356
-----------
My genotype at rs326: AA or (A;A)
rs326(A;A) is associated with: lower HDL cholesterol
rs326(A;G) is associated with: lower HDL cholesterol
rs326(G;G) is associated with: normal risk

357
-----------
My genotype at rs17482753: GG or (G;G)
rs17482753(G;G) is associated with: normal
rs17482753(G;T) is associated with: elevated triglycerides
rs17482753(T;T) is associated with: elevated triglycerides

358
-----------
My genotype at rs10503669: CC or (C;C)
rs10503669(A;A) is associated with: associated with higher HDL cholesterol
rs10503669(A;C) is associated with: associated with higher HDL cholesterol

359
-----------
My genotype at rs2270641: TT or (T;T)
rs2270641(G;G) is associated with: 3.7x higher risk for schizophrenia
rs2270641(G;T) is associated with: ?
rs2270641(T;T) is associated with: normal

360
-----------
My genotype at rs7014851: TT or (T;T)
rs7014851(C;C) is associated with: None
rs7014851(C;T) is associated with: None
rs7014851(T;T) is associated with: common

361
-----------
My genotype at rs11136000: TT or (T;T)
rs11136000(C;C) is associated with: normal
rs11136000(C;T) is associated with: 0.84x decreased risk for Alzheimer's disease
rs11136000(T;T) is associated with: 0.84x decreased risk for Alzheimer's disease

362
-----------
My genotype at rs2609653: TT or (T;T)
rs2609653(C;C) is associated with: 3.6x risk
rs2609653(C;T) is associated with: 1.5x risk
rs2609653(T;T) is associated with: normal

363
-----------
My genotype at rs4994: AA or (T;T)
rs4994(C;C) is associated with: 2x higher risk in certain women for cardiac events
rs4994(C;T) is associated with: 2x higher risk in certain women for cardiac events
rs4994(T;T) is associated with: normal

364
-----------
My genotype at rs7003908: CC or (C;C)
rs7003908(A;A) is associated with: normal
rs7003908(A;C) is associated with: normal
rs7003908(C;C) is associated with: 1.4x increased risk for glioblastoma

365
-----------
My genotype at rs2228063: AA or (A;A)
rs2228063(A;A) is associated with: common
rs2228063(A;G) is associated with: None
rs2228063(G;G) is associated with: None

366
-----------
My genotype at rs13266634: CC or (C;C)
rs13266634(C;C) is associated with: increased risk for type-2 diabetes
rs13266634(C;T) is associated with: increased risk for type-2 diabetes
rs13266634(T;T) is associated with: normal

367
-----------
My genotype at rs3802177: GG or (C;C)
rs3802177(C;C) is associated with: 1.16x increased risk for type-2 diabetes
rs3802177(C;T) is associated with: 1.16x increased risk for type-2 diabetes
rs3802177(T;T) is associated with: normal

368
-----------
My genotype at rs16901979: CC or (C;C)
rs16901979(A;A) is associated with: 1.5x increased risk for prostate cancer
rs16901979(A;C) is associated with: 1.5x increased risk for prostate cancer
rs16901979(C;C) is associated with: normal risk

369
-----------
My genotype at rs10505483: CC or (G;G)
rs10505483(A;A) is associated with: None
rs10505483(A;G) is associated with: None
rs10505483(G;G) is associated with: common

370
-----------
My genotype at rs6983267: GG or (G;G)
rs6983267(G;G) is associated with: 1.58x increased risk for prostate cancer; also other cancers
rs6983267(G;T) is associated with: 1.2x risk of prostate cancer
rs6983267(T;T) is associated with: average risk

371
-----------
My genotype at rs1447295: CC or (C;C)
rs1447295(A;A) is associated with: 1.7x increased risk of prostate cancer
rs1447295(A;C) is associated with: 1.4x increased risk of prostate cancer
rs1447295(C;C) is associated with: normal

372
-----------
My genotype at rs4242382: GG or (G;G)
rs4242382(A;A) is associated with: 1.7x increased risk for prostate cancer
rs4242382(A;G) is associated with: 1.7x increased risk for prostate cancer
rs4242382(G;G) is associated with: normal risk

373
-----------
My genotype at rs7017300: AA or (A;A)
rs7017300(A;A) is associated with: normal risk
rs7017300(A;C) is associated with: 1.7x increased risk for prostate cancer
rs7017300(C;C) is associated with: 1.7x increased risk for prostate cancer

374
-----------
My genotype at rs10090154: CC or (C;C)
rs10090154(C;C) is associated with: normal
rs10090154(C;T) is associated with: 1.4x increased risk for prostate cancer
rs10090154(T;T) is associated with: 1.4x increased risk for prostate cancer

375
-----------
My genotype at rs7837688: GG or (G;G)
rs7837688(G;G) is associated with: 1.7x increased risk for prostate cancer
rs7837688(G;T) is associated with: 1.7x increased risk for prostate cancer
rs7837688(T;T) is associated with: normal risk

376
-----------
My genotype at rs9642880: GG or (G;G)
rs9642880(G;G) is associated with: normal
rs9642880(G;T) is associated with: 1.2x increased bladder cancer risk
rs9642880(T;T) is associated with: 1.5x increased bladder cancer risk

377
-----------
My genotype at rs987525: CC or (C;C)
rs987525(A;A) is associated with: 6x increased risk for cleft lip
rs987525(A;C) is associated with: 2.5x increased risk for cleft lip
rs987525(C;C) is associated with: normal

378
-----------
My genotype at rs6997709: GG or (G;G)
rs6997709(G;G) is associated with: 1.5x higher risk for hypertension
rs6997709(G;T) is associated with: 1.2x higher risk for hypertension
rs6997709(T;T) is associated with: normal

379
-----------
My genotype at rs2294008: CC or (C;C)
rs2294008(T;T) is associated with: increased risk of gastric and bladder cancer

380
-----------
My genotype at rs2572886: GG or (G;G)
rs2572886(A;A) is associated with: 1.4x increased risk of HIV infection
rs2572886(A;G) is associated with: 1.4x increased risk of HIV infection
rs2572886(G;G) is associated with: normal

381
-----------
My genotype at rs9886784: CC or (C;C)
rs9886784(A;A) is associated with: >3.2x risk for AD
rs9886784(A;C) is associated with: 3.2x risk for AD
rs9886784(C;C) is associated with: average

382
-----------
My genotype at rs719725: CC or (C;C)
rs719725(A;A) is associated with: 1.46x increased risk for colorectal cancer
rs719725(A;C) is associated with: 1.5x increased risk for colorectal cancer
rs719725(C;C) is associated with: normal

383
-----------
My genotype at rs3814113: TT or (T;T)
rs3814113(C;C) is associated with: 0.8x decreased risk for ovarian cancer
rs3814113(C;T) is associated with: 0.8x decreased risk for ovarian cancer
rs3814113(T;T) is associated with: normal

384
-----------
My genotype at rs3731239: AA or (T;T)
rs3731239(C;C) is associated with: 0.9x lower risk for breast cancer
rs3731239(C;T) is associated with: ?
rs3731239(T;T) is associated with: normal risk

385
-----------
My genotype at rs3218005: TT or (A;A)
rs3218005(A;A) is associated with: 1.55x higher risk for breast cancer
rs3218005(A;G) is associated with: ?
rs3218005(G;G) is associated with: normal risk

386
-----------
My genotype at rs10811661: TT or (T;T)
rs10811661(C;C) is associated with: normal
rs10811661(C;T) is associated with: 1.2x increased risk for type-2 diabetes
rs10811661(T;T) is associated with: 1.2x increased risk for type-2 diabetes

387
-----------
My genotype at rs7019241: CC or (C;C)
rs7019241(C;C) is associated with: average
rs7019241(C;T) is associated with: reduced risk for AD?
rs7019241(T;T) is associated with: reduced risk for AD?

388
-----------
My genotype at rs10868366: GG or (G;G)
rs10868366(G;G) is associated with: average
rs10868366(G;T) is associated with: reduced risk for AD?
rs10868366(T;T) is associated with: reduced risk for AD?

389
-----------
My genotype at rs965513: GG or (G;G)
rs965513(A;A) is associated with: 3.5x increased thyroid cancer risk
rs965513(A;G) is associated with: 1.7x increased thyroid cancer risk
rs965513(G;G) is associated with: normal

390
-----------
My genotype at rs1867277: GG or (G;G)
rs1867277(A;A) is associated with: 2x increased risk for thyroid cancer
rs1867277(A;G) is associated with: 1.5x increased risk for thyroid cancer
rs1867277(G;G) is associated with: normal

391
-----------
My genotype at rs4149274: GG or (C;C)
rs4149274(C;C) is associated with: associated with higher HDL cholesterol
rs4149274(C;T) is associated with: associated with higher HDL cholesterol

392
-----------
My genotype at rs4149268: CC or (G;G)
rs4149268(A;G) is associated with: associated with higher HDL cholesterol
rs4149268(G;G) is associated with: associated with higher HDL cholesterol

393
-----------
My genotype at rs10759932: TT or (T;T)
rs10759932(C;C) is associated with: increased risk for chorionic plate inflammation
rs10759932(C;T) is associated with: increased risk for chorionic plate inflammation
rs10759932(T;T) is associated with: normal

394
-----------
My genotype at rs4986790: AA or (A;A)
rs4986790(A;A) is associated with: normal
rs4986790(A;G) is associated with: None
rs4986790(G;G) is associated with: complex; numerous associations reported

395
-----------
My genotype at rs4986791: CC or (C;C)
rs4986791(C;C) is associated with: normal
rs4986791(C;T) is associated with: complex; see details
rs4986791(T;T) is associated with: complex; see details

396
-----------
My genotype at rs1953126: CC or (C;C)
rs1953126(C;C) is associated with: normal
rs1953126(C;T) is associated with: 1.3x increased risk for rheumatoid arthritis
rs1953126(T;T) is associated with: 1.3x increased risk for rheumatoid arthritis

397
-----------
My genotype at rs1571801: TT or (A;A)
rs1571801(A;A) is associated with: >1.36x risk for prostate cancer
rs1571801(A;C) is associated with: 1.36x risk for prostate cancer
rs1571801(C;C) is associated with: average

398
-----------
My genotype at rs10306114: AA or (A;A)
rs10306114(A;A) is associated with: normal
rs10306114(A;G) is associated with: Higher risk of bleeding during coronary angiography
rs10306114(G;G) is associated with: Higher risk of bleeding during coronary angiography

399
-----------
My genotype at rs3842787: CC or (C;C)
rs3842787(C;C) is associated with: normal
rs3842787(C;T) is associated with: Higher risk of bleeding during coronary angiography
rs3842787(T;T) is associated with: Higher risk of bleeding during coronary angiography

400
-----------
My genotype at rs3003609: TT or (T;T)
rs3003609(C;C) is associated with: normal
rs3003609(C;T) is associated with: ?
rs3003609(T;T) is associated with: associated with heavier smoking in Caucasians

401
-----------
My genotype at rs2283123: CC or (C;C)
rs2283123(C;C) is associated with: normal risk of schizophrenia in limited study
rs2283123(C;T) is associated with: decreased risk of schizophrenia in limited study
rs2283123(T;T) is associated with: decreased risk of schizophrenia in limited study

402
-----------
My genotype at rs41309764: GG or (C;C)
rs41309764(C;C) is associated with: normal
rs41309764(C;T) is associated with: Congenital heart disease and valve calcification likely
rs41309764(T;T) is associated with: Congenital heart disease and valve calcification

403
-----------
My genotype at rs908832: GG or (G;G)
rs908832(A;A) is associated with: 3.8x increased risk for early-onset Alzheimers
rs908832(G;G) is associated with: normal

404
-----------
My genotype at rs6602024: GG or (G;G)
rs6602024(A;A) is associated with: 1-3 body mass index units heavier on average
rs6602024(A;G) is associated with: ?
rs6602024(G;G) is associated with: normal

405
-----------
My genotype at rs6601764: TT or (T;T)
rs6601764(C;C) is associated with: 1.5x risk
rs6601764(C;T) is associated with: 1.1x risk
rs6601764(T;T) is associated with: normal

406
-----------
My genotype at rs1800860: GG or (G;G)
rs1800860(A;A) is associated with: 10% smaller kidneys as newborns
rs1800860(A;G) is associated with: 10% smaller kidneys as newborns
rs1800860(G;G) is associated with: normal

407
-----------
My genotype at rs17158558: CC or (C;C)
rs17158558(C;C) is associated with: normal
rs17158558(C;T) is associated with: normal
rs17158558(T;T) is associated with: associated in just 1 case with Hirschsprung disease

408
-----------
My genotype at rs3026785: TT or (T;T)
rs3026785(C;C) is associated with: may be protective against Hirschsprung disease
rs3026785(C;T) is associated with: may be protective against Hirschsprung disease
rs3026785(T;T) is associated with: normal

409
-----------
My genotype at rs4253208: GG or (G;G)
rs4253208(C;C) is associated with: normal
rs4253208(C;G) is associated with: carrier
rs4253208(G;G) is associated with: possible COCKAYNE SYNDROME, TYPE B

410
-----------
My genotype at rs2177369: GG or (C;C)
rs2177369(C;C) is associated with: 1.5x increased risk for Alzheimer's disease
rs2177369(C;T) is associated with: normal
rs2177369(T;T) is associated with: normal

411
-----------
My genotype at rs10993994: CC or (C;C)
rs10993994(T;T) is associated with: 1.2x prostate cancer risk

412
-----------
My genotype at rs2279420: AA or (T;T)
rs2279420(C;C) is associated with: 0.79x decreased risk for LOAD
rs2279420(C;T) is associated with: 0.79x decreased risk for LOAD
rs2279420(T;T) is associated with: normal

413
-----------
My genotype at rs3758391: TT or (T;T)
rs3758391(C;C) is associated with: normal
rs3758391(C;T) is associated with: less mental decline with age
rs3758391(T;T) is associated with: less mental decline with age

414
-----------
My genotype at rs5030882: TT or (T;T)
rs5030882(C;T) is associated with: 
rs5030882(T;T) is associated with: common

415
-----------
My genotype at rs1049550: AA or (T;T)
rs1049550(C;C) is associated with: normal
rs1049550(C;T) is associated with: 0.62x reduced risk for sarcoidosis
rs1049550(T;T) is associated with: 0.62x reduced risk for sarcoidosis

416
-----------
My genotype at rs2274223: AA or (A;A)
rs2274223(A;A) is associated with: normal
rs2274223(A;G) is associated with: 1.5x increased risk for stomach & esophageal cancer (seen in Han Chinese)
rs2274223(G;G) is associated with: 1.9x increased risk for stomach & esophageal cancer (seen in Han Chinese)

417
-----------
My genotype at rs28399504: AA or (A;A)
rs28399504(A;A) is associated with: normal
rs28399504(A;G) is associated with: carrier
rs28399504(G;G) is associated with: poor metabolizer

418
-----------
My genotype at rs55752064: TT or (T;T)
rs55752064(C;C) is associated with: CYP2C19*14 homozygote
rs55752064(C;T) is associated with: carrier of one CYP2C19*14 allele
rs55752064(T;T) is associated with: normal

419
-----------
My genotype at rs17882687: AA or (A;A)
rs17882687(A;A) is associated with: normal
rs17882687(A;C) is associated with: carrier of one CYP2C19*15 allele
rs17882687(C;C) is associated with: CYP2C19*15 homozygote

420
-----------
My genotype at rs17878459: GG or (G;G)
rs17878459(C;C) is associated with: CYP2C19*2B homozygote
rs17878459(C;G) is associated with: carrier of one CYP2C19*2B allele
rs17878459(G;G) is associated with: normal

421
-----------
My genotype at rs41291556: TT or (T;T)
rs41291556(C;C) is associated with: CYP2C19*8 homozygote
rs41291556(C;T) is associated with: carrier of one CYP2C19*8 allele
rs41291556(T;T) is associated with: normal

422
-----------
My genotype at rs72552267: GG or (G;G)
rs72552267(A;A) is associated with: CYP2C19*6 homozygote
rs72552267(A;G) is associated with: carrier of one CYP2C19*6 allele
rs72552267(G;G) is associated with: normal

423
-----------
My genotype at rs17884712: GG or (G;G)
rs17884712(A;A) is associated with: CYP2C19*9 homozygote
rs17884712(A;G) is associated with: carrier of one CYP2C19*9 allele
rs17884712(G;G) is associated with: normal

424
-----------
My genotype at rs4986893: GG or (G;G)
rs4986893(A;A) is associated with: poor metabolizer of several commonly prescribed drugs
rs4986893(A;G) is associated with: carrier
rs4986893(G;G) is associated with: normal

425
-----------
My genotype at rs6413438: CC or (C;C)
rs6413438(C;C) is associated with: normal
rs6413438(C;T) is associated with: carrier of one CYP2C19*10 allele
rs6413438(T;T) is associated with: CYP2C19*10 homozygote

426
-----------
My genotype at rs72558186: TT or (T;T)
rs72558186(A;A) is associated with: CYP2C19*7 homozygote
rs72558186(A;T) is associated with: carrier of one CYP2C19*7 allele
rs72558186(T;T) is associated with: normal

427
-----------
My genotype at rs3758581: GG or (G;G)
rs3758581(A;A) is associated with: CYP2C19 V331I homozygote
rs3758581(A;G) is associated with: carrier of one CYP2C19 V331I allele
rs3758581(G;G) is associated with: normal

428
-----------
My genotype at rs17879685: CC or (C;C)
rs17879685(C;C) is associated with: normal
rs17879685(C;T) is associated with: carrier of one CYP2C19*13 allele
rs17879685(T;T) is associated with: CYP2C19*13 homozygote

429
-----------
My genotype at rs55640102: AA or (A;A)
rs55640102(A;A) is associated with: normal
rs55640102(A;C) is associated with: carrier of one CYP2C19*12 allele
rs55640102(C;C) is associated with: CYP2C19*12 homozygote

430
-----------
My genotype at rs1799853: CC or (C;C)
rs1799853(C;C) is associated with: normal; no change in warfarin metabolism
rs1799853(C;T) is associated with: CYP2C9*2 carrier; average 20% reduction in warfarin metabolism
rs1799853(T;T) is associated with: CYP2C9*2 homozygote; average 40% reduction in warfarin metabolism

431
-----------
My genotype at rs7900194: GG or (G;G)
rs7900194(A;A) is associated with: CYP2C9*8 homozygote
rs7900194(A;G) is associated with: carrier of one CYP2C9*8 allele
rs7900194(G;G) is associated with: normal

432
-----------
My genotype at rs72558190: CC or (C;C)
rs72558190(A;A) is associated with: CYP2C9*15 homozygote
rs72558190(A;C) is associated with: carrier of one CYP2C9*15 allele
rs72558190(C;C) is associated with: normal

433
-----------
My genotype at rs2256871: AA or (T;T)
rs2256871(C;C) is associated with: CYP2C9*9 homozygote
rs2256871(C;T) is associated with: carrier of one CYP2C9*9 allele
rs2256871(T;T) is associated with: normal

434
-----------
My genotype at rs9332130: AA or (A;A)
rs9332130(A;A) is associated with: normal
rs9332130(A;G) is associated with: carrier of one CYP2C9*10 allele
rs9332130(G;G) is associated with: CYP2C9*10 homozygote

435
-----------
My genotype at rs28371685: CC or (C;C)
rs28371685(C;C) is associated with: normal
rs28371685(C;T) is associated with: carrier of one CYP2C9*11 allele
rs28371685(T;T) is associated with: CYP2C9*11 homozygote

436
-----------
My genotype at rs1057909: AA or (A;A)
rs1057909(A;A) is associated with: normal
rs1057909(A;G) is associated with: carrier of one CYP2C9_42612A>G allele
rs1057909(G;G) is associated with: CYP2C9_42612A>G homozygote

437
-----------
My genotype at rs1057910: AA or (A;A)
rs1057910(A;A) is associated with: normal; no effect on warfarin metabolism
rs1057910(A;C) is associated with: CYP2C9*3 carrier; average 40% reduction in warfarin metabolism
rs1057910(C;C) is associated with: CYP2C9*3 homozygote; average 80% reduction in warfarin metabolism

438
-----------
My genotype at rs28371686: CC or (C;C)
rs28371686(G;G) is associated with: CYP2C9*5 homozygote
rs28371686(C;G) is associated with: carrier of one CYP2C9*5 allele
rs28371686(C;C) is associated with: normal

439
-----------
My genotype at rs1057911: AA or (T;T)
rs1057911(A;A) is associated with: CYP2C9_50298A>T homozygote
rs1057911(A;T) is associated with: carrier of one CYP2C9_50298A>T allele
rs1057911(T;T) is associated with: normal

440
-----------
My genotype at rs9332239: CC or (C;C)
rs9332239(C;C) is associated with: normal
rs9332239(C;T) is associated with: carrier of one CYP2C9*12 allele
rs9332239(T;T) is associated with: CYP2C9*12 homozygote

441
-----------
My genotype at rs2273697: GG or (G;G)
rs2273697(A;A) is associated with: Adverse reaction more likely to carbamazepine in epileptic patients
rs2273697(A;G) is associated with: Adverse reaction more likely to carbamazepine in epileptic patients
rs2273697(G;G) is associated with: normal/common

442
-----------
My genotype at rs2986017: AA or (T;T)
rs2986017(C;C) is associated with: normal
rs2986017(C;T) is associated with: no clear risk
rs2986017(T;T) is associated with: no clear risk

443
-----------
My genotype at rs4506565: AA or (T;T)
rs4506565(A;A) is associated with: 1.9x increased risk for type-2 diabetes
rs4506565(A;T) is associated with: 1.4x increased risk for type-2 diabetes
rs4506565(T;T) is associated with: normal

444
-----------
My genotype at rs7903146: CC or (C;C)
rs7903146(C;C) is associated with: normal form
rs7903146(C;T) is associated with: 1.4x increased risk for diabetes (and perhaps colon cancer)
rs7903146(T;T) is associated with: 2x increased risk for Type-2 diabetes

445
-----------
My genotype at rs12255372: GG or (G;G)
rs12255372(G;T) is associated with: 1.3x increased type-2 diabetes risk
rs12255372(T;T) is associated with: increased breast cancer, type-2 diabetes, and aggressive prostate cancer risk

446
-----------
My genotype at rs1801252: AA or (A;A)
rs1801252(A;A) is associated with: None
rs1801252(A;G) is associated with: 
rs1801252(G;G) is associated with: 

447
-----------
My genotype at rs11200014: GG or (G;G)
rs11200014(A;A) is associated with: 1.64x risk for breast cancer
rs11200014(A;G) is associated with: 1.20x risk for breast cancer
rs11200014(G;G) is associated with: common

448
-----------
My genotype at rs2981579: GG or (C;C)
rs2981579(C;C) is associated with: common
rs2981579(C;T) is associated with: 1.20x risk for breast cancer
rs2981579(T;T) is associated with: 1.64x risk for breast cancer

449
-----------
My genotype at rs1219648: AA or (A;A)
rs1219648(A;A) is associated with: 1.64x risk for breast cancer
rs1219648(A;G) is associated with: 1.20x risk for breast cancer
rs1219648(G;G) is associated with: common

450
-----------
My genotype at rs2420946: CC or (C;C)
rs2420946(C;C) is associated with: common
rs2420946(C;T) is associated with: 1.20x risk for breast cancer
rs2420946(T;T) is associated with: 1.64x risk for breast cancer

451
-----------
My genotype at rs2981582: GG or (C;C)
rs2981582(C;C) is associated with: normal
rs2981582(C;T) is associated with: 1.3x higher risk of ER+ breast cancer
rs2981582(T;T) is associated with: 1.7x higher risk of ER+ breast cancer

452
-----------
My genotype at rs10490924: GG or (G;G)
rs10490924(G;T) is associated with: 2.7x risk for age related macular degeneration
rs10490924(T;T) is associated with: 8.2x risk for age related macular degeneration

453
-----------
My genotype at rs2981745: TT or (T;T)
rs2981745(C;C) is associated with: normal
rs2981745(C;T) is associated with: 1.6x increased risk for breast cancer in females over 60
rs2981745(T;T) is associated with: >1.6x increased risk for breast cancer in females over 60

454
-----------
My genotype at rs11523871: CC or (C;C)
rs11523871(A;A) is associated with: normal
rs11523871(A;C) is associated with: 1.6x increased breast cancer risk for women over 60
rs11523871(C;C) is associated with: >1.6x increased breast cancer risk for women over 60

455
-----------
My genotype at rs2308327: AA or (A;A)
rs2308327(A;A) is associated with: normal
rs2308327(A;G) is associated with: 0.67x decreased risk for lung cancer
rs2308327(G;G) is associated with: 0.10x decreased risk for lung cancer

456
-----------
My genotype at rs3813867: GG or (G;G)
rs3813867(C;C) is associated with: CYP2E1_-1295G>C homozygote
rs3813867(C;G) is associated with: carrier of one CYP2E1_-1295G>C allele
rs3813867(G;G) is associated with: normal

457
-----------
My genotype at rs2031920: CC or (C;C)
rs2031920(C;C) is associated with: normal
rs2031920(C;T) is associated with: carrier of one CYP2E1_-1055C>T allele
rs2031920(T;T) is associated with: CYP2E1_-1055C>T homozygote

458
-----------
My genotype at rs2070672: AA or (A;A)
rs2070672(A;A) is associated with: CYP2E1*7_-352A>G homozygote
rs2070672(A;G) is associated with: carrier of one CYP2E1*7_-352A>G allele
rs2070672(G;G) is associated with: normal

459
-----------
My genotype at rs2070673: TT or (T;T)
rs2070673(A;A) is associated with: CYP2E1*7_-333T>A  homozygote
rs2070673(A;T) is associated with: carrier of one CYP2E1*7_-333T>A  allele
rs2070673(T;T) is associated with: normal

460
-----------
My genotype at rs6413420: GG or (G;G)
rs6413420(G;G) is associated with: normal
rs6413420(G;T) is associated with: carrier of one CYP2E1*7_-71G>T allele
rs6413420(T;T) is associated with: CYP2E1*7_-71G>T homozygote

461
-----------
My genotype at rs6413419: GG or (G;G)
rs6413419(A;A) is associated with: CYP2E1*4 homozygote
rs6413419(A;G) is associated with: carrier of one CYP2E1*4 allele
rs6413419(G;G) is associated with: normal

462
-----------
My genotype at rs915909: CC or (C;C)
rs915909(C;C) is associated with: normal
rs915909(C;T) is associated with: carrier of one CYP2E1_6498C>T(I321I) allele
rs915909(T;T) is associated with: CYP2E1_6498C>T(I321I) homozygote

463
-----------
My genotype at rs4646976: AA or (A;A)
rs4646976(A;A) is associated with: normal
rs4646976(A;G) is associated with: carrier of one CYP2E1_marker8 allele
rs4646976(G;G) is associated with: CYP2E1_marker8 homozygote

464
-----------
My genotype at rs2070676: CC or (G;G)
rs2070676(C;C) is associated with: CYP2E1*1B homozygote
rs2070676(C;G) is associated with: carrier of one CYP2E1*1B allele
rs2070676(G;G) is associated with: normal

465
-----------
My genotype at rs55897648: GG or (G;G)
rs55897648(A;A) is associated with: CYP2E1*3 homozygote
rs55897648(A;G) is associated with: carrier of one CYP2E1*3 allele
rs55897648(G;G) is associated with: normal

466
-----------
My genotype at rs2515641: CC or (C;C)
rs2515641(C;C) is associated with: CYP2E1_10463T>C(F421F) homozygote
rs2515641(C;T) is associated with: carrier of one CYP2E1_10463T>C(F421F) allele
rs2515641(T;T) is associated with: normal

467
-----------
My genotype at rs17571: GG or (C;C)
rs17571(T;T) is associated with: rare and doesn't seem helpful

468
-----------
My genotype at rs4320932: TT or (A;A)
rs4320932(A;A) is associated with: normal
rs4320932(A;G) is associated with: 0.87x decreased risk for ovarian cancer
rs4320932(G;G) is associated with: 0.74x decreased risk for ovarian cancer

469
-----------
My genotype at rs2237897: CC or (C;C)
rs2237897(C;C) is associated with: common
rs2237897(C;T) is associated with: 1.2x increased risk for diabetic nephropathy in some populations
rs2237897(T;T) is associated with: 1.4x increased risk for diabetic nephropathy in some populations

470
-----------
My genotype at rs34139813: CC or (G;G)
rs34139813(C;C) is associated with: Normal hemoglobin
rs34139813(C;G) is associated with: Heterozygous Hb Crete
rs34139813(G;G) is associated with: homozygous Hb Crete

471
-----------
My genotype at rs3781719: AA or (T;T)
rs3781719(C;C) is associated with: 2x increased hypertension risk
rs3781719(C;T) is associated with: 2x increased hypertension risk
rs3781719(T;T) is associated with: normal

472
-----------
My genotype at rs1793004: CC or (G;G)
rs1793004(C;C) is associated with: increased risk for Crohn's disease
rs1793004(C;G) is associated with: ?
rs1793004(G;G) is associated with: 0.89x decreased risk for Crohn's disease

473
-----------
My genotype at rs8192466: GG or (C;C)
rs8192466(C;C) is associated with: common
rs8192466(C;T) is associated with: None
rs8192466(T;T) is associated with: None

474
-----------
My genotype at rs10835638: GG or (G;G)
rs10835638(G;G) is associated with: common
rs10835638(G;T) is associated with: intermediate serum FSH level among males
rs10835638(T;T) is associated with: lower serum FSH level among males

475
-----------
My genotype at rs9300039: CC or (C;C)
rs9300039(A;A) is associated with: normal risk
rs9300039(A;C) is associated with: 1.5x risk for T2D
rs9300039(C;C) is associated with: >1.5x risk for T2D

476
-----------
My genotype at rs10897346: CC or (C;C)
rs10897346(C;C) is associated with: if depressed, 2.6x more likely to not respond to antidepressants
rs10897346(C;T) is associated with: if depressed, 2.6x more likely to not respond to antidepressants
rs10897346(T;T) is associated with: normal

477
-----------
My genotype at rs569108: AA or (T;T)
rs569108(C;C) is associated with: ?
rs569108(C;T) is associated with: 3x risk
rs569108(T;T) is associated with: normal

478
-----------
My genotype at rs931127: AA or (A;A)
rs931127(A;A) is associated with: 2.15x more likely positive lymph node
rs931127(G;G) is associated with: more favorable

479
-----------
My genotype at rs2448490: GG or (G;G)
rs2448490(A;A) is associated with: 0.57x (reduced) risk for metastasis in LN-/ER+ breast cancer patients
rs2448490(A;G) is associated with: normal
rs2448490(G;G) is associated with: normal

480
-----------
My genotype at rs1695: GG or (G;G)
rs1695(A;A) is associated with: normal asthma risk in certain populations
rs1695(A;G) is associated with: ?
rs1695(G;G) is associated with: 3.5x asthma risk in certain populations

481
-----------
My genotype at rs3736228: CC or (C;C)
rs3736228(C;C) is associated with: normal
rs3736228(C;T) is associated with: increased risk for osteoporosis
rs3736228(T;T) is associated with: increased risk for osteoporosis

482
-----------
My genotype at rs603965: GG or (G;G)
rs603965(A;A) is associated with: normal
rs603965(A;G) is associated with: ?
rs603965(G;G) is associated with: increased breast cancer risk

483
-----------
My genotype at rs7101429: AA or (A;A)
rs7101429(A;A) is associated with: higher Alzheimer's risk if ApoE4 also present
rs7101429(A;G) is associated with: 0.70x reduced risk for Alzheimer's risk
rs7101429(G;G) is associated with: 0.70x reduced risk for Alzheimer's risk

484
-----------
My genotype at rs2373115: CC or (G;G)
rs2373115(G;T) is associated with: normal
rs2373115(T;T) is associated with: normal

485
-----------
My genotype at rs1126809: GG or (G;G)
rs1126809(A;A) is associated with: slight increase in skin cancer risk
rs1126809(A;G) is associated with: slight increase in skin cancer risk
rs1126809(G;G) is associated with: normal

486
-----------
My genotype at rs10830963: CC or (G;G)
rs10830963(C;C) is associated with: normal
rs10830963(C;G) is associated with: increased type-2 diabetes risk
rs10830963(G;G) is associated with: increased type-2 diabetes risk

487
-----------
My genotype at rs1042838: CC or (G;G)
rs1042838(G;G) is associated with: normal risk
rs1042838(G;T) is associated with: 1.26x risk for ovarian cancer
rs1042838(T;T) is associated with: 3.2x risk for ovarian cancer

488
-----------
My genotype at rs12184413: CC or (C;C)
rs12184413(C;C) is associated with: normal
rs12184413(C;T) is associated with: normal
rs12184413(T;T) is associated with: 0.7x decreased risk for breast cancer

489
-----------
My genotype at rs1800054: CC or (G;G)
rs1800054(C;G) is associated with: very slightly  increased risk (1.05) for breast cancer
rs1800054(G;G) is associated with: 1.5x increased risk for breast cancer

490
-----------
My genotype at rs4986761: TT or (T;T)
rs4986761(C;C) is associated with: 1.5x increased risk for breast cancer
rs4986761(C;T) is associated with: very slightly  increased risk (1.05) for breast cancer
rs4986761(T;T) is associated with: normal

491
-----------
My genotype at rs1800056: TT or (T;T)
rs1800056(C;C) is associated with: 1.5x increased risk for breast cancer
rs1800056(C;T) is associated with: very slightly  increased risk (1.05) for breast cancer
rs1800056(T;T) is associated with: normal

492
-----------
My genotype at rs1800057: CC or (G;G)
rs1800057(C;G) is associated with: very slightly  increased risk (1.05) for breast cancer
rs1800057(G;G) is associated with: 1.5x increased risk for breast cancer

493
-----------
My genotype at rs1800058: CC or (C;C)
rs1800058(C;T) is associated with: very slightly  increased risk (1.05) for breast cancer
rs1800058(T;T) is associated with: 1.5x increased risk for breast cancer

494
-----------
My genotype at rs1801516: GG or (G;G)
rs1801516(A;A) is associated with: 2.76x odds of pancreatic cancer
rs1801516(A;G) is associated with: normal
rs1801516(G;G) is associated with: normal

495
-----------
My genotype at rs664143: GG or (C;C)
rs664143(C;C) is associated with: normal
rs664143(C;T) is associated with: 1.6x increased risk of lung cancer
rs664143(T;T) is associated with: 1.6x increased risk of lung cancer

496
-----------
My genotype at rs187238: CC or (G;G)
rs187238(C;C) is associated with: hypertension not a risk factor for sudden cardiac death
rs187238(C;G) is associated with: hypertension not a risk factor for sudden cardiac death
rs187238(G;G) is associated with: hypertension increases risk 3.75x for sudden cardiac death

497
-----------
My genotype at rs6277: AA or (T;T)
rs6277(C;C) is associated with: 1.6x higher schizophrenia risk
rs6277(C;T) is associated with: 1.4x higher schizophrenia risk
rs6277(T;T) is associated with: learns NoGo faster

498
-----------
My genotype at rs1801028: GG or (C;C)
rs1801028(G;G) is associated with: normal risk
rs1801028(C;G) is associated with: 1.4x risk for schizophrenia
rs1801028(C;C) is associated with: normal risk

499
-----------
My genotype at rs1076560: CC or (C;C)
rs1076560(A;A) is associated with: influences working memory
rs1076560(A;C) is associated with: 1.3x increased risk for alcoholism
rs1076560(C;C) is associated with: normal

500
-----------
My genotype at rs4648317: GG or (C;C)
rs4648317(C;C) is associated with: normal
rs4648317(C;T) is associated with: prone to higher nicotine dependence?
rs4648317(T;T) is associated with: prone to higher nicotine dependence?

501
-----------
My genotype at rs2075291: CC or (C;C)
rs2075291(A;A) is associated with: >4x higher risk for high triglyceride levels in Asians
rs2075291(A;C) is associated with: 4x higher risk for high triglyceride levels in Asians
rs2075291(C;C) is associated with: normal

502
-----------
My genotype at rs662799: AA or (A;A)
rs662799(A;A) is associated with: normal
rs662799(A;G) is associated with: less weight gain on high fat diets
rs662799(G;G) is associated with: less weight gain on high fat diets

503
-----------
My genotype at rs5092: TT or (A;A)
rs5092(A;A) is associated with: less likely to gain weight if taking olanzapine
rs5092(A;G) is associated with: less likely to gain weight if taking olanzapine
rs5092(G;G) is associated with: normal

504
-----------
My genotype at rs28931573: GG or (C;C)
rs28931573(C;T) is associated with: positive for the APOA1 Milano variant
rs28931573(T;T) is associated with: homozygous for the APOA1 Milano variant

505
-----------
My genotype at rs1954787: TT or (T;T)
rs1954787(C;C) is associated with: ~10% more likely to respond to citalopram
rs1954787(C;T) is associated with: normal risk
rs1954787(T;T) is associated with: ~10% less likely to respond to citalopram

506
-----------
My genotype at rs1699103: CC or (G;G)
rs1699103(A;A) is associated with: normal
rs1699103(A;G) is associated with: normal
rs1699103(G;G) is associated with: 0.85x risk for Alzheimers

507
-----------
My genotype at rs11218350: TT or (T;T)
rs11218350(A;A) is associated with: normal
rs11218350(A;T) is associated with: normal
rs11218350(T;T) is associated with: 0.83x risk for Alzheimers

508
-----------
My genotype at rs10892759: GG or (G;G)
rs10892759(A;A) is associated with: 0.83x risk for Alzheimers
rs10892759(A;G) is associated with: normal
rs10892759(G;G) is associated with: normal

509
-----------
My genotype at rs1792113: GG or (G;G)
rs1792113(A;A) is associated with: normal
rs1792113(A;G) is associated with: normal
rs1792113(G;G) is associated with: 0.90x risk for Alzheimers

510
-----------
My genotype at rs726601: CC or (C;C)
rs726601(C;C) is associated with: normal
rs726601(C;T) is associated with: normal
rs726601(T;T) is associated with: 0.86x risk for Alzheimers

511
-----------
My genotype at rs1784931: AA or (A;A)
rs1784931(A;A) is associated with: normal
rs1784931(A;C) is associated with: normal
rs1784931(C;C) is associated with: 0.86x risk for Alzheimers

512
-----------
My genotype at rs10893081: TT or (T;T)
rs10893081(C;C) is associated with: 2x increased risk for severe atherosclerosis; 1.2x increased risk for ischemic heart disease
rs10893081(C;T) is associated with: normal
rs10893081(T;T) is associated with: normal

513
-----------
My genotype at rs521102: GG or (C;C)
rs521102(C;C) is associated with: normal
rs521102(C;T) is associated with: normal
rs521102(T;T) is associated with: pancreatic cancer patients respond poorer to combined therapy

514
-----------
My genotype at rs2298566: CC or (C;C)
rs2298566(A;A) is associated with: normal
rs2298566(A;C) is associated with: increased risk of coronary heart disease; better response to statins
rs2298566(C;C) is associated with: increased risk of coronary heart disease; better response to statins

515
-----------
My genotype at rs12425791: GG or (G;G)
rs12425791(A;A) is associated with: possibly increased risk of stroke
rs12425791(A;G) is associated with: mixed evidence of increased risk for stroke
rs12425791(G;G) is associated with: normal

516
-----------
My genotype at rs5443: TT or (T;T)
rs5443(C;C) is associated with: higher risk for several conditions
rs5443(C;T) is associated with: (some risk; see details)
rs5443(T;T) is associated with: sibutramine has no effect

517
-----------
My genotype at rs1805762: CC or (G;G)
rs1805762(C;C) is associated with: >1.23x risk for hypertension
rs1805762(C;G) is associated with: 1.23x risk for hypertension
rs1805762(G;G) is associated with: average

518
-----------
My genotype at rs669: TT or (A;A)
rs669(A;A) is associated with: normal
rs669(A;G) is associated with: possibly increased risk for Alzheimers
rs669(G;G) is associated with: 3.8x or higher increased risk for Alzheimers

519
-----------
My genotype at rs11052552: GG or (G;G)
rs11052552(G;G) is associated with: 1.4x risk
rs11052552(G;T) is associated with: 1.5x risk
rs11052552(T;T) is associated with: normal

520
-----------
My genotype at rs11045585: AA or (A;A)
rs11045585(A;A) is associated with: 24% chance (lower than average) of docetaxel-induced leukopenia/neutropenia
rs11045585(A;G) is associated with: 63% chance (higher than average) of docetaxel-induced leukopenia/neutropenia
rs11045585(G;G) is associated with: (no data; implied high chance of docetaxel-induced leukopenia/neutropenia)

521
-----------
My genotype at rs4149056: TT or (T;T)
rs4149056(C;C) is associated with: 17x myopathy risk for statin users
rs4149056(C;T) is associated with: reduced breakdown of some drugs; 5x increased myopathy risk for statin users
rs4149056(T;T) is associated with: normal

522
-----------
My genotype at rs4363657: TT or (T;T)
rs4363657(C;C) is associated with: 17x increased myopathy risk for statin users
rs4363657(C;T) is associated with: 4.5x increased myopathy risk for statin users
rs4363657(T;T) is associated with: normal

523
-----------
My genotype at rs7961152: CC or (C;C)
rs7961152(A;A) is associated with: 1.5x higher risk for hypertension
rs7961152(A;C) is associated with: 1.2x higher risk for hypertension
rs7961152(C;C) is associated with: normal

524
-----------
My genotype at rs33949390: GG or (G;G)
rs33949390(C;C) is associated with: 3.3x increased risk for Parkinson's disease
rs33949390(C;G) is associated with: 3.3x increased risk for Parkinson's disease
rs33949390(G;G) is associated with: normal

525
-----------
My genotype at rs34637584: GG or (G;G)
rs34637584(A;A) is associated with: 15 to 30% chance of Parkinson's disease, depending on age, family history, and ethnicity
rs34637584(A;G) is associated with: 15 to 30% chance of Parkinson's disease, depending on age, family history, and ethnicity
rs34637584(G;G) is associated with: normal

526
-----------
My genotype at rs34778348: GG or (G;G)
rs34778348(A;A) is associated with: 2.1x increased risk for Parkinson's disease
rs34778348(A;G) is associated with: 2.1x increased risk for Parkinson's disease
rs34778348(G;G) is associated with: normal

527
-----------
My genotype at rs2107301: GG or (C;C)
rs2107301(C;C) is associated with: normal risk
rs2107301(C;T) is associated with: ?
rs2107301(T;T) is associated with: 2.5x higher risk for prostate cancer

528
-----------
My genotype at rs4516035: TT or (T;T)
rs4516035(C;C) is associated with: if less milk in teenage females, less bone?
rs4516035(C;T) is associated with: if less milk in teenage females, less bone?
rs4516035(T;T) is associated with: normal

529
-----------
My genotype at rs3736309: AA or (A;A)
rs3736309(A;A) is associated with: normal
rs3736309(A;G) is associated with: 0.44x decreased risk for chronic obstructive pulmonary lung disease
rs3736309(G;G) is associated with: 0.44x decreased risk for chronic obstructive pulmonary lung disease

530
-----------
My genotype at rs12304921: AA or (A;A)
rs12304921(A;A) is associated with: normal
rs12304921(A;G) is associated with: 2.5x risk
rs12304921(G;G) is associated with: 1.9x risk

531
-----------
My genotype at rs60554162: CC or (G;G)
rs60554162(A;A) is associated with: homozygote for pachyonyitia congenita Type I mutation
rs60554162(A;G) is associated with: heterozygote for pachyonychia congenita Type I mutation
rs60554162(G;G) is associated with: normal

532
-----------
My genotype at rs57052654: AA or (T;T)
rs57052654(G;G) is associated with: homozygote for pachyonychia congenita Type I mutation
rs57052654(G;T) is associated with: heterozygote for pachyonychia congenita Type I mutation
rs57052654(T;T) is associated with: normal

533
-----------
My genotype at rs28933087: AA or (T;T)
rs28933087(G;G) is associated with: homozygote for pachyonychia congenita Type I mutation
rs28933087(G;T) is associated with: heterozygote for pachyonychia congenita Type I mutation
rs28933087(T;T) is associated with: normal

534
-----------
My genotype at rs11614913: CC or (C;C)
rs11614913(C;C) is associated with: increased risk of various types of cancer
rs11614913(C;T) is associated with: normal
rs11614913(T;T) is associated with: normal

535
-----------
My genotype at rs4570625: GG or (G;G)
rs4570625(G;G) is associated with: higher scores on anxiety-related personality traits; greater placebo response
rs4570625(G;T) is associated with: normal
rs4570625(T;T) is associated with: normal

536
-----------
My genotype at rs4565946: CC or (C;C)
rs4565946(C;C) is associated with: Risk of early-onset OCD
rs4565946(T;T) is associated with: None

537
-----------
My genotype at rs7305115: AA or (A;A)
rs7305115(A;A) is associated with: Individuals showed a significantly lower risk of suicide behavior than those with the A/G or G/G genotype
rs7305115(A;G) is associated with: risk of suicide behavior
rs7305115(G;G) is associated with: risk of suicide behavior

538
-----------
My genotype at rs1545843: AA or (A;A)
rs1545843(A;A) is associated with: 1.4x increased risk for depression (for those under 55)
rs1545843(G;G) is associated with: normal

539
-----------
My genotype at rs3782179: TT or (T;T)
rs3782179(C;T) is associated with: 3x increased testicular cancer risk for men

540
-----------
My genotype at rs4474514: AA or (A;A)
rs4474514(A;A) is associated with: >3x increased testicular cancer risk for men
rs4474514(A;G) is associated with: 3x increased testicular cancer risk for men
rs4474514(G;G) is associated with: normal

541
-----------
My genotype at rs11110912: CC or (G;G)
rs11110912(C;C) is associated with: 1.3x risk
rs11110912(C;G) is associated with: 1.3x risk
rs11110912(G;G) is associated with: normal

542
-----------
My genotype at rs28934899: CC or (G;G)
rs28934899(G;G) is associated with: normal

543
-----------
My genotype at rs5030849: CC or (G;G)
rs5030849(A;A) is associated with: PHENYLKETONURIA, MILD
rs5030849(A;G) is associated with: PHENYLKETONURIA, MILD

544
-----------
My genotype at rs1522305: GG or (G;G)
rs1522305(C;C) is associated with: normal
rs1522305(C;G) is associated with: normal
rs1522305(G;G) is associated with: slightly increased risk for schizophrenia

545
-----------
My genotype at rs6539137: TT or (T;T)
rs6539137(A;A) is associated with: increased risk for and earlier onset in males of familial ALS
rs6539137(A;T) is associated with: 
rs6539137(T;T) is associated with: normal

546
-----------
My genotype at rs3794260: GG or (G;G)
rs3794260(A;A) is associated with: >1.26x risk for hypertension
rs3794260(A;G) is associated with: 1.26x risk for hypertension
rs3794260(G;G) is associated with: average

547
-----------
My genotype at rs3184504: TT or (T;T)
rs3184504(C;C) is associated with: normal
rs3184504(C;T) is associated with: increased risk for celiac disease
rs3184504(T;T) is associated with: increased risk for celiac disease

548
-----------
My genotype at rs671: GG or (G;G)
rs671(A;A) is associated with: Flusher, increased risk of esophageal cancer
rs671(A;G) is associated with: experiences asian flush
rs671(G;G) is associated with: normal

549
-----------
My genotype at rs5888: AA or (T;T)
rs5888(C;C) is associated with: normal
rs5888(C;T) is associated with: 3x higher risk for age-related macular degeneration
rs5888(T;T) is associated with: 1.6x higher risk for age-related macular degeneration

550
-----------
My genotype at rs1027557: TT or (A;A)
rs1027557(A;G) is associated with: heterozygosity seems common

551
-----------
My genotype at rs2306536: CC or (C;C)
rs2306536(C;C) is associated with: average
rs2306536(C;T) is associated with: ?
rs2306536(T;T) is associated with: 0.5x lower risk of colorectal cancer

552
-----------
My genotype at rs9550642: GG or (G;G)
rs9550642(A;A) is associated with: 2.2x risk
rs9550642(A;G) is associated with: 1.3x risk
rs9550642(G;G) is associated with: normal

553
-----------
My genotype at rs4076128: AA or (A;A)
rs4076128(A;A) is associated with: 1.8x increased breast cancer risk for women having high linoleic acid diets
rs4076128(A;G) is associated with: normal
rs4076128(G;G) is associated with: normal

554
-----------
My genotype at rs10507391: TT or (T;T)
rs10507391(A;A) is associated with: normal
rs10507391(A;T) is associated with: 1.24x increased stroke risk for males
rs10507391(T;T) is associated with: 1.24x increased stroke risk for males

555
-----------
My genotype at rs144848: AA or (T;T)
rs144848(G;G) is associated with: 1.3x increased risk for breast cancer
rs144848(G;T) is associated with: possible increased risk for breast cancer
rs144848(T;T) is associated with: normal

556
-----------
My genotype at rs28897756: GG or (G;G)
rs28897756(A;A) is associated with: possible link to breast cancer in some families
rs28897756(A;G) is associated with: possible link to breast cancer in some families
rs28897756(G;G) is associated with: normal

557
-----------
My genotype at rs211239: GG or (C;C)
rs211239(C;C) is associated with: 1.7x risk for priapism in SCA patients
rs211239(C;T) is associated with: 1.7x risk for priapism in SCA patients
rs211239(T;T) is associated with: normal risk for priapism in SCA patients

558
-----------
My genotype at rs6314: GG or (C;C)
rs6314(C;C) is associated with: higher risk for RA
rs6314(C;T) is associated with: higher risk for RA; better response to paroxetine as treatment for depression
rs6314(T;T) is associated with: average

559
-----------
My genotype at rs7997012: AA or (A;A)
rs7997012(A;A) is associated with: ~18% more likely to respond to citalopram
rs7997012(A;G) is associated with: normal risk
rs7997012(G;G) is associated with: ~18% less likely to respond to citalopram

560
-----------
My genotype at rs1328674: CC or (G;G)
rs1328674(A;A) is associated with: higher risk for RA
rs1328674(A;G) is associated with: higher risk for RA
rs1328674(G;G) is associated with: average

561
-----------
My genotype at rs2854344: GG or (G;G)
rs2854344(A;A) is associated with: normal risk
rs2854344(A;G) is associated with: 
rs2854344(G;G) is associated with: 1.25x risk of developing ovarian cancer

562
-----------
My genotype at rs10492519: AA or (A;A)
rs10492519(A;A) is associated with: normal risk
rs10492519(A;G) is associated with: somewhat higher risk for prostate cancer
rs10492519(G;G) is associated with: somewhat higher risk for prostate cancer

563
-----------
My genotype at rs5352: CC or (G;G)
rs5352(A;A) is associated with: probably [[Hirschsprung disease]]
rs5352(A;G) is associated with: probably [[Hirschsprung disease]] carrier
rs5352(G;G) is associated with: common

564
-----------
My genotype at rs7326018: AA or (T;T)
rs7326018(A;A) is associated with: normal
rs7326018(A;T) is associated with: normal
rs7326018(T;T) is associated with: 1.8x increased risk for multiple sclerosis

565
-----------
My genotype at rs1327328: AA or (T;T)
rs1327328(C;C) is associated with: normal
rs1327328(C;T) is associated with: normal
rs1327328(T;T) is associated with: 1.7x increased risk for multiple sclerosis

566
-----------
My genotype at rs9589207: GG or (G;G)
rs9589207(A;A) is associated with: None
rs9589207(A;G) is associated with: None
rs9589207(G;G) is associated with: common

567
-----------
My genotype at rs1805097: TT or (A;A)
rs1805097(A;A) is associated with: twice as likely to reach extreme old age?
rs1805097(A;G) is associated with: normal
rs1805097(G;G) is associated with: normal

568
-----------
My genotype at rs1154155: TT or (T;T)
rs1154155(G;G) is associated with: 2.5x increased risk for narcolepsy
rs1154155(G;T) is associated with: 1.94x increased risk for narcolepsy
rs1154155(T;T) is associated with: normal

569
-----------
My genotype at rs1048990: CC or (G;G)
rs1048990(C;C) is associated with: > 1.48x risk
rs1048990(C;G) is associated with: 1.48x risk
rs1048990(G;G) is associated with: common

570
-----------
My genotype at rs10498345: TT or (T;T)
rs10498345(A;A) is associated with: <0.5x decreased risk for coronary spasm
rs10498345(A;T) is associated with: 0.5x decreased risk for coronary spasm
rs10498345(T;T) is associated with: normal

571
-----------
My genotype at rs10134944: CC or (C;C)
rs10134944(C;C) is associated with: normal
rs10134944(C;T) is associated with: 1.4x risk
rs10134944(T;T) is associated with: 1.3x risk

572
-----------
My genotype at rs767603: CC or (C;C)
rs767603(C;C) is associated with: 0.63x reduced risk for intracranial aneurysm
rs767603(C;T) is associated with: normal
rs767603(T;T) is associated with: normal

573
-----------
My genotype at rs3783799: CC or (G;G)
rs3783799(A;A) is associated with: 1.4x increased risk for stroke
rs3783799(A;G) is associated with: 1.4x increased risk for stroke
rs3783799(G;G) is associated with: normal risk

574
-----------
My genotype at rs2230500: GG or (G;G)
rs2230500(A;A) is associated with: 1.4x increased risk for stroke
rs2230500(A;G) is associated with: 1.4x increased risk for stroke
rs2230500(G;G) is associated with: normal risk

575
-----------
My genotype at rs3025786: TT or (T;T)
rs3025786(C;C) is associated with: slightly decreased Alzheimer's disease risk among ApoE4 carriers
rs3025786(C;T) is associated with: slightly decreased Alzheimer's disease risk among ApoE4 carriers
rs3025786(T;T) is associated with: normal

576
-----------
My genotype at rs910316: AA or (T;T)
rs910316(G;G) is associated with: 0.68cm taller on average
rs910316(G;T) is associated with: 0.34cm taller on average
rs910316(T;T) is associated with: normal

577
-----------
My genotype at rs28929474: CC or (G;G)
rs28929474(A;A) is associated with: Alpha-1 Antitrypsin Deficiency
rs28929474(A;G) is associated with: carrier for Alpha-1 Antitrypsin Deficiency

578
-----------
My genotype at rs28931568: CC or (G;G)
rs28931568(A;A) is associated with: high risk of emphysema

579
-----------
My genotype at rs28931569: AA or (T;T)
rs28931569(C;C) is associated with: high risk of emphysema

580
-----------
My genotype at rs7158782: AA or (A;A)
rs7158782(A;A) is associated with: normal
rs7158782(A;G) is associated with: 2x higher risk of adverse side-effect if taking aromatase inhibitor
rs7158782(G;G) is associated with: 4x higher risk of adverse side-effect if taking aromatase inhibitor

581
-----------
My genotype at rs8702: GG or (G;G)
rs8702(C;C) is associated with: average
rs8702(C;G) is associated with: ?
rs8702(G;G) is associated with: 0.2x risk for MS

582
-----------
My genotype at rs1800407: CC or (G;G)
rs1800407(A;A) is associated with: green/hazel/brown/black eyes more likely
rs1800407(A;G) is associated with: green/hazel/brown/black eyes more likely
rs1800407(G;G) is associated with: blue/gray eyes more possible

583
-----------
My genotype at rs1800401: GG or (C;C)
rs1800401(C;C) is associated with: blue/gray eyes possible
rs1800401(C;T) is associated with: brown/black eyes more likely
rs1800401(T;T) is associated with: brown/black eyes more likely

584
-----------
My genotype at rs4778138: AA or (A;A)
rs4778138(A;A) is associated with: freckles more likely

585
-----------
My genotype at rs4778241: CC or (C;C)
rs4778241(A;A) is associated with: usually brown eye color
rs4778241(A;C) is associated with: usually brown eye color
rs4778241(C;C) is associated with: blue eye color if part of blue eye color haplotype

586
-----------
My genotype at rs7495174: AA or (A;A)
rs7495174(A;A) is associated with: blue/gray eyes more likely
rs7495174(A;G) is associated with: blue/gray eyes less likely
rs7495174(G;G) is associated with: blue/gray eyes less likely

587
-----------
My genotype at rs1129038: TT or (A;A)
rs1129038(A;A) is associated with: brown eye color
rs1129038(A;G) is associated with: brown eye color
rs1129038(G;G) is associated with: blue eye color

588
-----------
My genotype at rs12593929: AA or (A;A)
rs12593929(A;A) is associated with: brown eye color
rs12593929(A;G) is associated with: brown eye color
rs12593929(G;G) is associated with: blue eye color if part of blue eye color haplotype

589
-----------
My genotype at rs12913832: GG or (G;G)
rs12913832(A;A) is associated with: brown eye color, 80% of the time
rs12913832(A;G) is associated with: brown eye color
rs12913832(G;G) is associated with: blue eye color, 99% of the time

590
-----------
My genotype at rs7183877: CC or (C;C)
rs7183877(A;A) is associated with: usually brown eye color
rs7183877(A;C) is associated with: usually brown eye color
rs7183877(C;C) is associated with: blue eye color if part of blue eye color haplotype

591
-----------
My genotype at rs3935591: CC or (G;G)
rs3935591(A;A) is associated with: usually brown eye color
rs3935591(A;G) is associated with: usually brown eye color
rs3935591(G;G) is associated with: blue eye color if part of blue eye color haplotype

592
-----------
My genotype at rs8028689: TT or (T;T)
rs8028689(C;C) is associated with: usually brown eye color
rs8028689(C;T) is associated with: usually brown eye color
rs8028689(T;T) is associated with: blue eye color if part of blue eye color haplotype

593
-----------
My genotype at rs2240203: TT or (A;A)
rs2240203(A;A) is associated with: usually brown eye color
rs2240203(A;G) is associated with: usually brown eye color
rs2240203(G;G) is associated with: blue eye color if part of blue eye color haplotype

594
-----------
My genotype at rs916977: CC or (G;G)
rs916977(A;A) is associated with: usually brown eye color
rs916977(A;G) is associated with: usually brown eye color
rs916977(G;G) is associated with: blue eye color if part of blue eye color haplotype

595
-----------
My genotype at rs4779584: CC or (C;C)
rs4779584(C;C) is associated with: average
rs4779584(C;T) is associated with: 1.23x risk for colorectal cancer
rs4779584(T;T) is associated with: 1.70x risk for colorectal cancer

596
-----------
My genotype at rs11073328: CC or (C;C)
rs11073328(C;C) is associated with: normal
rs11073328(T;T) is associated with: increased longevity?

597
-----------
My genotype at rs748404: CC or (C;C)
rs748404(C;T) is associated with: very slightly  increased risk (1.15) for lung cancer
rs748404(T;T) is associated with: slightly  increased risk (1.25) for lung cancer

598
-----------
My genotype at rs1426654: AA or (A;A)
rs1426654(A;A) is associated with: probably light-skinned, European ancestry
rs1426654(A;G) is associated with: mixed African/European ancestry possible
rs1426654(G;G) is associated with: probably darker-skinned, Asian or African ancestry

599
-----------
My genotype at rs4775041: GG or (G;G)
rs4775041(C;C) is associated with: lowest phosphatidylethanolamine values
rs4775041(C;G) is associated with: intermediate phosphatidylethanolamine values
rs4775041(G;G) is associated with: highest phosphatidylethanolamine values

600
-----------
My genotype at rs10468017: CC or (C;C)
rs10468017(C;T) is associated with: associated with higher HDL cholesterol
rs10468017(T;T) is associated with: associated with higher HDL cholesterol

601
-----------
My genotype at rs3825776: TT or (A;A)
rs3825776(A;A) is associated with: average
rs3825776(A;G) is associated with: 1.3x risk for ALS
rs3825776(G;G) is associated with: >1.3x risk for ALS

602
-----------
My genotype at rs2073711: GG or (C;C)
rs2073711(C;C) is associated with: higher risk of LDD
rs2073711(C;T) is associated with: higher risk of LDD
rs2073711(T;T) is associated with: average

603
-----------
My genotype at rs17228212: TT or (T;T)
rs17228212(C;C) is associated with: >1.26x increased risk for heart disease
rs17228212(C;T) is associated with: 1.26x increased risk for heart disease
rs17228212(T;T) is associated with: normal

604
-----------
My genotype at rs8038652: GG or (G;G)
rs8038652(A;A) is associated with: shorter adult height, at least among Mongolians
rs8038652(A;G) is associated with: normal
rs8038652(G;G) is associated with: normal

605
-----------
My genotype at rs28940871: GG or (G;G)
rs28940871(C;G) is associated with: Tay-Sachs carrier
rs28940871(G;G) is associated with: Tay-Sachs disease likely; see details

606
-----------
My genotype at rs3825942: GG or (C;C)
rs3825942(C;C) is associated with: common but 10x higher glaucoma risk
rs3825942(C;T) is associated with: possibly higher glaucoma risk?
rs3825942(T;T) is associated with: average

607
-----------
My genotype at rs2930291: GG or (C;C)
rs2930291(C;C) is associated with: 1.5x risk
rs2930291(C;T) is associated with: 1.3x risk
rs2930291(T;T) is associated with: normal

608
-----------
My genotype at rs2069526: TT or (T;T)
rs2069526(G;G) is associated with: CYP1A2*1K_-739T>G homozygote
rs2069526(G;T) is associated with: carrier of one CYP1A2*1K_-739T>G allele
rs2069526(T;T) is associated with: normal

609
-----------
My genotype at rs12720461: CC or (C;C)
rs12720461(C;C) is associated with: normal
rs12720461(C;T) is associated with: carrier of one CYP1A2*1K_-729C>T allele
rs12720461(T;T) is associated with: CYP1A2*1K_-729C>T homozygote

610
-----------
My genotype at rs762551: AA or (A;A)
rs762551(A;A) is associated with: CYP1A2*1F homozygote; Fast metabolizer
rs762551(A;C) is associated with: carrier of one CYP1A2*1F allele; slow metabolizer
rs762551(C;C) is associated with: CYP1A2 slow metabolizer

611
-----------
My genotype at rs72547513: AA or (A;A)
rs72547513(A;A) is associated with: CYP1A2*11 homozygote
rs72547513(A;C) is associated with: carrier of one CYP1A2*11 allele
rs72547513(C;C) is associated with: normal

612
-----------
My genotype at rs56276455: GG or (G;G)
rs56276455(A;A) is associated with: CYP1A2*3 homozygote
rs56276455(A;G) is associated with: carrier of one CYP1A2*3 allele
rs56276455(G;G) is associated with: normal

613
-----------
My genotype at rs72547515: GG or (C;C)
rs72547515(T;T) is associated with: CYP1A2*16 homozygote
rs72547515(C;T) is associated with: carrier of one CYP1A2*16 allele
rs72547515(C;C) is associated with: normal

614
-----------
My genotype at rs72547516: AA or (A;A)
rs72547516(T;T) is associated with: CYP1A2*4 homozygote
rs72547516(A;T) is associated with: carrier of one CYP1A2*4 allele
rs72547516(A;A) is associated with: normal

615
-----------
My genotype at rs55889066: GG or (G;G)
rs55889066(A;A) is associated with: CYP1A2*5 homozygote
rs55889066(A;G) is associated with: carrier of one CYP1A2*5 allele
rs55889066(G;G) is associated with: normal

616
-----------
My genotype at rs28399424: CC or (C;C)
rs28399424(C;C) is associated with: normal
rs28399424(C;T) is associated with: carrier of one CYP1A2*6 allele
rs28399424(T;T) is associated with: CYP1A2*6 homozygote

617
-----------
My genotype at rs72547517: GG or (G;G)
rs72547517(A;A) is associated with: CYP1A2*8 homozygote
rs72547517(A;G) is associated with: carrier of one CYP1A2*8 allele
rs72547517(G;G) is associated with: normal

618
-----------
My genotype at rs2470890: TT or (T;T)
rs2470890(C;C) is associated with: CYP1A2_1545T>C homozygote
rs2470890(C;T) is associated with: carrier of one CYP1A2_1545T>C allele
rs2470890(T;T) is associated with: normal

619
-----------
My genotype at rs9652490: GG or (G;G)
rs9652490(A;A) is associated with: ~2x increased risk for Parkinson's disease, and, essential tremor
rs9652490(A;G) is associated with: likely (slight?) increased risk for Parkinson's disease
rs9652490(G;G) is associated with: normal

620
-----------
My genotype at rs2398162: AA or (A;A)
rs2398162(A;A) is associated with: 1.3x risk
rs2398162(A;G) is associated with: normal
rs2398162(G;G) is associated with: normal

621
-----------
My genotype at rs34516635: GG or (G;G)
rs34516635(G;G) is associated with: normal
rs34516635(A;G) is associated with: longevity effect?
rs34516635(A;A) is associated with: longevity effect?

622
-----------
My genotype at rs28940577: TT or (A;A)
rs28940577(A;G) is associated with: FAMILIAL MEDITERRANEAN FEVER carrier
rs28940577(G;G) is associated with: FAMILIAL MEDITERRANEAN FEVER

623
-----------
My genotype at rs725613: TT or (A;A)
rs725613(A;A) is associated with: 1.2x increased type-1 diabetes risk; 1.2x increased multiple sclerosis risk
rs725613(A;C) is associated with: 1.2x increased type-1 diabetes risk; 1.2x increased multiple sclerosis risk
rs725613(C;C) is associated with: normal

624
-----------
My genotype at rs12708716: AA or (A;A)
rs12708716(A;A) is associated with: 1.6x risk
rs12708716(A;G) is associated with: 1.2x risk
rs12708716(G;G) is associated with: normal

625
-----------
My genotype at rs6498169: GG or (G;G)
rs6498169(A;A) is associated with: >1.14x risk
rs6498169(A;G) is associated with: 1.14x risk
rs6498169(G;G) is associated with: common

626
-----------
My genotype at rs13333226: AA or (A;A)
rs13333226(A;A) is associated with: common but slightly higher risk for hypertension
rs13333226(A;G) is associated with: slightly lower risk for hypertension
rs13333226(G;G) is associated with: ~15-20% lower risk for hypertension or cardiovascular events

627
-----------
My genotype at rs420259: AA or (T;T)
rs420259(C;C) is associated with: normal
rs420259(C;T) is associated with: 2x risk
rs420259(T;T) is associated with: 2x risk

628
-----------
My genotype at rs8050894: CC or (G;G)
rs8050894(C;C) is associated with: warfarin sensitivity (~2.5 mg/day)
rs8050894(G;G) is associated with: warfarin resistance (~6.5 mg/day)

629
-----------
My genotype at rs9923231: CC or (C;C)
rs9923231(C;C) is associated with: normal
rs9923231(C;T) is associated with: reduced warfarin dose if treated for VTE
rs9923231(T;T) is associated with: reduced warfarin dose if treated for VTE

630
-----------
My genotype at rs12597511: CC or (C;C)
rs12597511(C;C) is associated with: normal
rs12597511(C;T) is associated with: slightly higher blood pressure
rs12597511(T;T) is associated with: slightly higher blood pressure

631
-----------
My genotype at rs1143679: GG or (G;G)
rs1143679(A;A) is associated with: >1.78x increased risk for SLE
rs1143679(A;G) is associated with: 1.78x increased risk for SLE
rs1143679(G;G) is associated with: normal

632
-----------
My genotype at rs17822931: CC or (C;C)
rs17822931(C;C) is associated with: wet earwax
rs17822931(C;T) is associated with: wet earwax
rs17822931(T;T) is associated with: dry earwax

633
-----------
My genotype at rs17221417: GG or (G;G)
rs17221417(C;C) is associated with: normal
rs17221417(C;G) is associated with: 1.3x risk
rs17221417(G;G) is associated with: 1.9x risk

634
-----------
My genotype at rs2076756: GG or (G;G)
rs2076756(A;A) is associated with: normal
rs2076756(A;G) is associated with: ?
rs2076756(G;G) is associated with: 1.7x increased risk for Crohn's disease

635
-----------
My genotype at rs3803662: GG or (C;C)
rs3803662(C;C) is associated with: normal
rs3803662(C;T) is associated with: ?
rs3803662(T;T) is associated with: 1.6x increased risk for breast cancer

636
-----------
My genotype at rs3785143: CC or (C;C)
rs3785143(C;C) is associated with: normal risk of ADHD
rs3785143(C;T) is associated with: may be associated with ADHD
rs3785143(T;T) is associated with: may be associated with ADHD

637
-----------
My genotype at rs5558: TT or (T;T)
rs5558(G;G) is associated with: None
rs5558(T;T) is associated with: normal

638
-----------
My genotype at rs183130: CC or (C;C)
rs183130(C;C) is associated with: lower HDL cholesterol
rs183130(C;T) is associated with: lower HDL cholesterol
rs183130(T;T) is associated with: normal risk

639
-----------
My genotype at rs3764261: CC or (G;G)
rs3764261(G;T) is associated with: associated with higher HDL cholesterol
rs3764261(T;T) is associated with: associated with higher HDL cholesterol

640
-----------
My genotype at rs1864163: AA or (A;A)
rs1864163(A;G) is associated with: associated with higher HDL cholesterol
rs1864163(G;G) is associated with: associated with higher HDL cholesterol

641
-----------
My genotype at rs5882: AA or (A;A)
rs5882(A;G) is associated with: lower risk of dementia and Alzheimer's disease
rs5882(G;G) is associated with: longer lifespan, 0.28x lower risk of dementia, 0.31x lower risk of Alzheimer's.

642
-----------
My genotype at rs16260: CC or (C;C)
rs16260(A;A) is associated with: 2.6x increased risk of prostate cancer
rs16260(A;C) is associated with: 1.5-1.7x increased risk of prostate cancer
rs16260(C;C) is associated with: normal

643
-----------
My genotype at rs1061646: GG or (C;C)
rs1061646(C;C) is associated with: 1.16x increased risk for breast cancer
rs1061646(C;T) is associated with: 1.08x increased risk for breast cancer
rs1061646(T;T) is associated with: normal risk

644
-----------
My genotype at rs1805007: CC or (C;C)
rs1805007(C;C) is associated with: normal risk
rs1805007(C;T) is associated with: increased response to anesthetics
rs1805007(T;T) is associated with: increased response to anesthetics; 13-20x higher likelihood of red hair

645
-----------
My genotype at rs1805008: CC or (C;C)
rs1805008(C;T) is associated with: None
rs1805008(T;T) is associated with: ~7-10x higher likelihood of red hair

646
-----------
My genotype at rs28940279: AA or (A;A)
rs28940279(A;C) is associated with: carrier for Canavan disease
rs28940279(C;C) is associated with: Canavan disease

647
-----------
My genotype at rs28940574: CC or (C;C)
rs28940574(A;A) is associated with: Canavan disease
rs28940574(A;C) is associated with: carrier for Canavan disease

648
-----------
My genotype at rs34210653: GG or (C;C)
rs34210653(T;T) is associated with: normal risk
rs34210653(C;T) is associated with: 1.6x increased risk for heart disease
rs34210653(C;C) is associated with: normal risk

649
-----------
My genotype at rs12150220: TT or (T;T)
rs12150220(A;A) is associated with: slightly increased risk for several autoimmune diseases
rs12150220(A;T) is associated with: slightly increased risk for several autoimmune diseases
rs12150220(T;T) is associated with: normal

650
-----------
My genotype at rs2670660: GG or (G;G)
rs2670660(A;A) is associated with: normal
rs2670660(A;G) is associated with: 2.96x
rs2670660(G;G) is associated with: 2.74x

651
-----------
My genotype at rs6259: GG or (G;G)
rs6259(A;A) is associated with: normal
rs6259(A;G) is associated with: normal
rs6259(G;G) is associated with: best inverse correlation between tea-drinking, soy-consuming premenopausal women and risk of endometrial cancer

652
-----------
My genotype at rs1042522: CC or (G;G)
rs1042522(C;C) is associated with: longer lifespan?
rs1042522(C;G) is associated with: None

653
-----------
My genotype at rs4792311: GG or (G;G)
rs4792311(A;A) is associated with: increased risk of prostate cancer
rs4792311(A;G) is associated with: increased risk
rs4792311(G;G) is associated with: normal

654
-----------
My genotype at rs1889018: AA or (T;T)
rs1889018(C;C) is associated with: normal
rs1889018(C;T) is associated with: 1.12x increased risk for T2D
rs1889018(T;T) is associated with: 1.12x increased risk for T2D

655
-----------
My genotype at rs25532: GG or (C;C)
rs25532(C;C) is associated with: may be part of a haplotype associated with OCD
rs25532(C;T) is associated with: may be part of a haplotype associated with OCD
rs25532(T;T) is associated with: normal

656
-----------
My genotype at rs25531: CC or (G;G)
rs25531(A;A) is associated with: less happy
rs25531(G;G) is associated with: happier

657
-----------
My genotype at rs1050565: CC or (G;G)
rs1050565(A;A) is associated with: normal
rs1050565(A;G) is associated with: normal
rs1050565(G;G) is associated with: if testicular cancer patient, 5x poorer response to bleomycin chemotherapy

658
-----------
My genotype at rs4430796: AA or (A;A)
rs4430796(A;A) is associated with: 1.38x increased risk for prostate cancer
rs4430796(A;G) is associated with: normal risk
rs4430796(G;G) is associated with: normal risk

659
-----------
My genotype at rs8069176: GG or (G;G)
rs8069176(A;A) is associated with: normal
rs8069176(A;G) is associated with: normal
rs8069176(G;G) is associated with: if 4 years old or younger, ~3x increased asthma risk if exposed to smoke

660
-----------
My genotype at rs2305480: GG or (C;C)
rs2305480(C;C) is associated with: normal
rs2305480(C;T) is associated with: normal
rs2305480(T;T) is associated with: if 4 years old or younger, ~3x increased asthma risk if exposed to smoke

661
-----------
My genotype at rs4795400: CC or (C;C)
rs4795400(C;C) is associated with: normal
rs4795400(C;T) is associated with: normal
rs4795400(T;T) is associated with: if 4 years old or younger, ~2.5x increased asthma risk if exposed to smoke

662
-----------
My genotype at rs7216389: TT or (T;T)
rs7216389(C;C) is associated with: normal
rs7216389(C;T) is associated with: 1.5x increased risk for asthma
rs7216389(T;T) is associated with: 2.1x increased risk for asthma

663
-----------
My genotype at rs59328451: TT or (T;T)
rs59328451(A;A) is associated with: normal
rs59328451(A;T) is associated with: heterozygote for pachyonychia congenita Type I mutation
rs59328451(T;T) is associated with: homozygote for pachyonychia congenita Type I mutation

664
-----------
My genotype at rs28928895: AA or (T;T)
rs28928895(A;T) is associated with: heterozygote for pachyonychia congenita Type I mutation
rs28928895(T;T) is associated with: normal

665
-----------
My genotype at rs57424749: CC or (G;G)
rs57424749(C;C) is associated with: homozygote for pachyonychia congenita Type I mutation
rs57424749(C;G) is associated with: heterozygote for pachyonychia congenita Type I mutation
rs57424749(G;G) is associated with: normal

666
-----------
My genotype at rs58293603: AA or (T;T)
rs58293603(G;G) is associated with: homozygote for pachyonychia congenita Type I mutation
rs58293603(G;T) is associated with: heterozygote for pachyonychia congenita Type I mutation
rs58293603(T;T) is associated with: normal

667
-----------
My genotype at rs59349773: TT or (A;A)
rs59349773(A;A) is associated with: normal
rs59349773(A;C) is associated with: heterozygote for pachyonychia congenita Type I mutation
rs59349773(C;C) is associated with: homozygote for pachyonychia congenita Type I mutation

668
-----------
My genotype at rs28928894: AA or (T;T)
rs28928894(C;C) is associated with: homozygote for pachyonychia congenita Type I mutation
rs28928894(C;T) is associated with: heterozygote for pachyonychia congenita Type I mutation
rs28928894(T;T) is associated with: normal

669
-----------
My genotype at rs6503691: CC or (C;C)
rs6503691(C;C) is associated with: common
rs6503691(C;T) is associated with: None
rs6503691(T;T) is associated with: None

670
-----------
My genotype at rs28897696: GG or (C;C)
rs28897696(A;A) is associated with: carrier of two copies of BRCA1 variant; likely to be at higher risk for breast/ovarian cancer
rs28897696(A;C) is associated with: carrier of BRCA1 variant
rs28897696(C;C) is associated with: normal

671
-----------
My genotype at rs55770810: GG or (C;C)
rs55770810(C;C) is associated with: normal
rs55770810(C;T) is associated with: carrier of BRCA1 variant
rs55770810(T;T) is associated with: carrier of two copies of BRCA1 variant; likely to be at higher risk for breast/ovarian cancer

672
-----------
My genotype at rs41293455: GG or (C;C)
rs41293455(C;C) is associated with: normal
rs41293455(C;T) is associated with: possible predisposition to breast cancer
rs41293455(T;T) is associated with: predisposition to breast cancer?

673
-----------
My genotype at rs4986852: CC or (G;G)
rs4986852(A;A) is associated with: predisposition to breast cancer?
rs4986852(A;G) is associated with: possible predisposition to breast cancer
rs4986852(G;G) is associated with: normal

674
-----------
My genotype at rs1800709: GG or (C;C)
rs1800709(C;C) is associated with: normal
rs1800709(C;T) is associated with: possible predisposition to breast cancer
rs1800709(T;T) is associated with: predisposition to breast cancer?

675
-----------
My genotype at rs28897672: AA or (T;T)
rs28897672(G;G) is associated with: predisposition to breast cancer?
rs28897672(G;T) is associated with: possible predisposition to breast cancer
rs28897672(T;T) is associated with: normal

676
-----------
My genotype at rs242941: CC or (G;G)
rs242941(G;G) is associated with: better response to inhaled corticosteroid in patients with COPD
rs242941(G;T) is associated with: normal
rs242941(T;T) is associated with: normal

677
-----------
My genotype at rs5917: GG or (G;G)
rs5917(A;A) is associated with: None
rs5917(A;G) is associated with: None
rs5917(G;G) is associated with: common

678
-----------
My genotype at rs4794067: TT or (T;T)
rs4794067(C;C) is associated with: 2.1x risk for AIA
rs4794067(C;T) is associated with: 2.1x risk for AIA
rs4794067(T;T) is associated with: common

679
-----------
My genotype at rs2240017: CC or (G;G)
rs2240017(C;C) is associated with: not observed (too rare)
rs2240017(C;G) is associated with: respond better to steroids
rs2240017(G;G) is associated with: common

680
-----------
My genotype at rs2074190: AA or (T;T)
rs2074190(C;C) is associated with: 2.2x risk for AIA
rs2074190(C;T) is associated with: 2.2x risk for AIA
rs2074190(T;T) is associated with: common

681
-----------
My genotype at rs11650354: CC or (C;C)
rs11650354(C;C) is associated with: 8x risk for allergic asthma
rs11650354(C;T) is associated with: possible risk for allergic asthma
rs11650354(T;T) is associated with: common

682
-----------
My genotype at rs16947078: AA or (A;A)
rs16947078(A;A) is associated with: common
rs16947078(A;G) is associated with: possible risk for allergic asthma
rs16947078(G;G) is associated with: 8x risk for allergic asthma

683
-----------
My genotype at rs4968451: AA or (A;A)
rs4968451(A;A) is associated with: 1.5x increased risk for meningioma
rs4968451(A;C) is associated with: 1.5x increased risk for meningioma
rs4968451(C;C) is associated with: normal

684
-----------
My genotype at rs7213516: GG or (G;G)
rs7213516(A;A) is associated with: higher cardiovascular risk in African Americans
rs7213516(A;G) is associated with: higher cardiovascular risk in African Americans
rs7213516(G;G) is associated with: normal

685
-----------
My genotype at rs4290: CC or (C;C)
rs4290(C;C) is associated with: normal
rs4290(C;T) is associated with: higher cardiovascular risk in African Americans
rs4290(T;T) is associated with: higher cardiovascular risk in African Americans

686
-----------
My genotype at rs1859962: GG or (G;G)
rs1859962(G;G) is associated with: 1.28x increased risk for prostate cancer
rs1859962(G;T) is associated with: normal risk
rs1859962(T;T) is associated with: normal risk

687
-----------
My genotype at rs9951307: GG or (G;G)
rs9951307(A;A) is associated with: normal
rs9951307(A;G) is associated with: 0.10 decreased risk for brain edema after a stroke
rs9951307(G;G) is associated with: 0.10 decreased risk for brain edema after a stroke

688
-----------
My genotype at rs4464148: TT or (T;T)
rs4464148(C;C) is associated with: 1.35x increased risk for colorectal cancer
rs4464148(C;T) is associated with: 1.10x increased risk for colorectal cancer
rs4464148(T;T) is associated with: 1x normal risk for colorectal cancer

689
-----------
My genotype at rs4939883: CC or (C;C)
rs4939883(C;C) is associated with: associated with higher HDL cholesterol
rs4939883(C;T) is associated with: associated with higher HDL cholesterol

690
-----------
My genotype at rs9960767: AA or (A;A)
rs9960767(A;A) is associated with: normal
rs9960767(A;C) is associated with: 1.2x increased risk for schizophrenia
rs9960767(C;C) is associated with: 1.4x increased risk for schizophrenia

691
-----------
My genotype at rs17782313: TT or (T;T)
rs17782313(C;C) is associated with: adults likely to be 0.44 BMI units higher
rs17782313(C;T) is associated with: adults likely to be 0.22 BMI units higher
rs17782313(T;T) is associated with: normal

692
-----------
My genotype at rs10871777: AA or (A;A)
rs10871777(A;A) is associated with: adults likely to be 0.44 BMI units higher
rs10871777(A;G) is associated with: adults likely to be 0.22 BMI units higher
rs10871777(G;G) is associated with: normal

693
-----------
My genotype at rs12970134: GG or (G;G)
rs12970134(A;A) is associated with: adult waist 1.8cm larger on average
rs12970134(A;G) is associated with: adult waist 0.9cm larger on average
rs12970134(G;G) is associated with: normal

694
-----------
My genotype at rs2229616: CC or (G;G)
rs2229616(A;A) is associated with: lower risk of metabolic syndrome
rs2229616(A;G) is associated with: lower risk of metabolic syndrome
rs2229616(G;G) is associated with: normal

695
-----------
My genotype at rs763361: TT or (T;T)
rs763361(C;C) is associated with: normal
rs763361(C;T) is associated with: somewhat increased risk for multiple autoimmune diseases
rs763361(T;T) is associated with: somewhat increased risk for multiple autoimmune diseases

696
-----------
My genotype at rs11569562: AA or (T;T)
rs11569562(C;C) is associated with: increased risk for adult asthma
rs11569562(C;T) is associated with: ?
rs11569562(T;T) is associated with: normal

697
-----------
My genotype at rs2230199: GG or (G;G)
rs2230199(C;C) is associated with: 3.2x risk of ARMD
rs2230199(C;G) is associated with: 1.6x risk of ARMD
rs2230199(G;G) is associated with: common

698
-----------
My genotype at rs2305795: AA or (A;A)
rs2305795(A;A) is associated with: 1.3x risk of narcolepsy compared to (A;G) genotype
rs2305795(A;G) is associated with: normal risk of narcolepsy
rs2305795(G;G) is associated with: 0.75x risk of narcolepsy compared to (A;G) genotype

699
-----------
My genotype at rs1799969: GG or (G;G)
rs1799969(A;A) is associated with: slightly higher breast cancer risk
rs1799969(A;G) is associated with: slightly higher breast cancer risk
rs1799969(G;G) is associated with: normal

700
-----------
My genotype at rs5496: GG or (G;G)
rs5496(G;G) is associated with: common for caucasians, despite hapmap

701
-----------
My genotype at rs892086: AA or (T;T)
rs892086(C;C) is associated with: normal
rs892086(C;T) is associated with: normal
rs892086(T;T) is associated with: 1.5x increased Alzheimer risk in non-ApoE4 carriers

702
-----------
My genotype at rs28942079: GG or (G;G)
rs28942079(A;A) is associated with: risk of hypercholesterolemia
rs28942079(A;G) is associated with: None

703
-----------
My genotype at rs688: CC or (C;C)
rs688(C;C) is associated with: normal risk
rs688(C;T) is associated with: normal risk for Alzheimer's; higher total and LDL cholesterol in females
rs688(T;T) is associated with: 1.5x higher risk for males of Alzheimer's; higher total and LDL cholesterol in females

704
-----------
My genotype at rs1043994: CC or (G;G)
rs1043994(A;A) is associated with: ?
rs1043994(A;G) is associated with: ?
rs1043994(G;G) is associated with: common

705
-----------
My genotype at rs2108622: CC or (C;C)
rs2108622(C;C) is associated with: lower warfarin dosing
rs2108622(C;T) is associated with: None
rs2108622(T;T) is associated with: higher warfarin dosing

706
-----------
My genotype at rs10411210: CC or (C;C)
rs10411210(T;T) is associated with: 1.15x increased risk of colorectal cancer

707
-----------
My genotype at rs12979860: TT or (T;T)
rs12979860(C;C) is associated with: ~80% of such hepatitis C patients respond to treatment
rs12979860(C;T) is associated with: ~20-40% of such hepatitis C patients respond to treatment
rs12979860(T;T) is associated with: ~20-25% of such hepatitis C patients respond to treatment

708
-----------
My genotype at rs11881940: AA or (T;T)
rs11881940(A;A) is associated with: normal form
rs11881940(A;T) is associated with: 1.9x risk of MI
rs11881940(T;T) is associated with: 1.9x risk of MI

709
-----------
My genotype at rs1800469: GG or (C;C)
rs1800469(C;C) is associated with: higher risk for COPD
rs1800469(C;T) is associated with: higher risk for COPD
rs1800469(T;T) is associated with: normal risk

710
-----------
My genotype at rs25489: CC or (G;G)
rs25489(A;A) is associated with: 4.68x higher risk for breast cancer
rs25489(A;G) is associated with: normal risk
rs25489(G;G) is associated with: normal risk

711
-----------
My genotype at rs1799782: GG or (C;C)
rs1799782(C;C) is associated with: lower risk for skin cancer
rs1799782(C;T) is associated with: 1.3x increased risk for oral cancer among Asians
rs1799782(T;T) is associated with: 1.4x increased risk for oral cancer among Asians

712
-----------
My genotype at rs2075650: AA or (A;A)
rs2075650(A;A) is associated with: normal
rs2075650(A;G) is associated with: 2x higher Alzheimer's risk
rs2075650(G;G) is associated with: 4x higher Alzheimer's risk

713
-----------
My genotype at rs440446: GG or (G;G)
rs440446(C;C) is associated with: normal
rs440446(C;G) is associated with: increased risk in men for biliary conditions
rs440446(G;G) is associated with: increased risk in men for biliary conditions

714
-----------
My genotype at rs429358: TT or (T;T)
rs429358(C;C) is associated with: one of 2 snps relevant to classifying APOE genotype
rs429358(C;T) is associated with: >3x increased risk for Alzheimer's; 1.4x increased risk for heart disease
rs429358(T;T) is associated with: common

715
-----------
My genotype at rs7412: CC or (C;C)
rs7412(C;C) is associated with: more likely to gain weight if taking olanzapine
rs7412(C;T) is associated with: more likely to gain weight if taking olanzapine
rs7412(T;T) is associated with: normal

716
-----------
My genotype at rs1800437: GG or (G;G)
rs1800437(C;C) is associated with: average
rs1800437(C;G) is associated with: 0.72x risk for heart disease
rs1800437(G;G) is associated with: average

717
-----------
My genotype at rs1047781: AA or (T;T)
rs1047781(A;A) is associated with: ABH blood group "Secretor" status if Japanese
rs1047781(A;T) is associated with: ABH blood group "Secretor" status if Japanese
rs1047781(T;T) is associated with: ABH blood group "Non-Secretor" status if Japanese

718
-----------
My genotype at rs2295490: AA or (A;A)
rs2295490(A;A) is associated with: normal
rs2295490(A;G) is associated with: 1.32x increased risk of early-onset type-2 diabetes
rs2295490(G;G) is associated with: 1.32x increased risk of early-onset type-2 diabetes

719
-----------
My genotype at rs543749: TT or (T;T)
rs543749(G;G) is associated with: if a smoker, somewhat more likely to develop COPD

720
-----------
My genotype at rs16991615: GG or (G;G)
rs16991615(A;A) is associated with: age at menopause increased by avg of 22 months 
rs16991615(A;G) is associated with: slight increase (11 months) in avg age at menopause

721
-----------
My genotype at rs910873: GG or (G;G)
rs910873(A;A) is associated with: 3x increased risk of melanoma
rs910873(A;G) is associated with: 1.7x increased risk of melanoma
rs910873(G;G) is associated with: normal

722
-----------
My genotype at rs3746444: AA or (T;T)
rs3746444(C;C) is associated with: 1.25x increased risk for breast cancer
rs3746444(C;T) is associated with: 1.25x increased risk for breast cancer
rs3746444(T;T) is associated with: normal

723
-----------
My genotype at rs867186: AA or (A;A)
rs867186(A;A) is associated with: normal risk for VTE
rs867186(A;G) is associated with: EPCR H3 haplotype; reduced or increased risk of VTE?
rs867186(G;G) is associated with: EPCR H3 diplotype; reduced or increased risk of VTE?

724
-----------
My genotype at rs6013029: GG or (G;G)
rs6013029(G;G) is associated with: normal
rs6013029(G;T) is associated with: None
rs6013029(T;T) is associated with: None

725
-----------
My genotype at rs2250889: CC or (G;G)
rs2250889(C;C) is associated with: 1.69x higher risk for lung cancer
rs2250889(C;G) is associated with: 1.46x higher risk for lung cancer
rs2250889(G;G) is associated with: normal risk

726
-----------
My genotype at rs2230782: GG or (G;G)
rs2230782(C;C) is associated with: 0.45x reduced risk for breast cancer

727
-----------
My genotype at rs2834167: GG or (G;G)
rs2834167(A;A) is associated with: 2.67x increased risk for systemic sclerosis
rs2834167(A;G) is associated with: normal
rs2834167(G;G) is associated with: normal

728
-----------
My genotype at rs2837960: TT or (T;T)
rs2837960(G;G) is associated with: 2.3x risk
rs2837960(G;T) is associated with: normal
rs2837960(T;T) is associated with: normal

729
-----------
My genotype at rs2839471: TT or (T;T)
rs2839471(C;C) is associated with: normal
rs2839471(C;T) is associated with: 1.6x increased risk for high myopia
rs2839471(T;T) is associated with: 1.6x increased risk for high myopia

730
-----------
My genotype at rs9306160: CC or (C;C)
rs9306160(C;C) is associated with: normal
rs9306160(C;T) is associated with: 0.75x (reduced) risk for metastasis in LN-/ER+ breast cancer patients
rs9306160(T;T) is associated with: 0.75x (reduced) risk for metastasis in LN-/ER+ breast cancer patients

731
-----------
My genotype at rs6267: GG or (G;G)
rs6267(G;G) is associated with: common
rs6267(G;T) is associated with: None
rs6267(T;T) is associated with: None

732
-----------
My genotype at rs2267012: GG or (G;G)
rs2267012(A;A) is associated with: 1.3x increased risk for depression
rs2267012(A;G) is associated with: 1.3x increased risk for depression
rs2267012(G;G) is associated with: normal risk

733
-----------
My genotype at rs131690: GG or (G;G)
rs131690(A;A) is associated with: normal risk
rs131690(A;G) is associated with: 1.5x increased risk for bipolar disorder
rs131690(G;G) is associated with: 1.5x increased risk for bipolar disorder

734
-----------
My genotype at rs131702: GG or (G;G)
rs131702(G;T) is associated with: 
rs131702(T;T) is associated with: normal risk

735
-----------
My genotype at rs5751876: TT or (T;T)
rs5751876(C;C) is associated with: None
rs5751876(C;T) is associated with: None
rs5751876(T;T) is associated with: significantly higher anxiety levels after moderate caffeine consumption

736
-----------
My genotype at rs688034: CC or (C;C)
rs688034(C;C) is associated with: normal
rs688034(C;T) is associated with: 1.1x risk
rs688034(T;T) is associated with: 1.6x risk

737
-----------
My genotype at rs663048: GG or (G;G)
rs663048(G;G) is associated with: None
rs663048(G;T) is associated with: None
rs663048(T;T) is associated with: 3x risk of with [[lung cancer]]

738
-----------
My genotype at rs2071746: AA or (T;T)
rs2071746(A;A) is associated with: normal
rs2071746(A;T) is associated with: normal
rs2071746(T;T) is associated with: may be part of gs124

739
-----------
My genotype at rs743777: AA or (A;A)
rs743777(A;A) is associated with: 1.7x risk
rs743777(A;G) is associated with: 1.1x risk
rs743777(G;G) is associated with: normal

740
-----------
My genotype at rs2072797: CC or (C;C)
rs2072797(C;C) is associated with: normal
rs2072797(C;T) is associated with: 1.5x increased risk of Non-Hodgkin Lymphoma
rs2072797(T;T) is associated with: 1.5x increased risk of Non-Hodgkin Lymphoma

741
-----------
My genotype at rs1135840: GG or (G;G)
rs1135840(C;C) is associated with: Homozygous for CYP2D6 variants (non-CYP2D6*1)
rs1135840(C;G) is associated with: Carrier of at least one CYP2D6 variants (non-CYP2D6*1)
rs1135840(G;G) is associated with: normal

742
-----------
My genotype at rs28371733: CC or (G;G)
rs28371733(A;A) is associated with: Homozygous for CYP2D6*52 variant.
rs28371733(A;G) is associated with: Carrier of one CYP2D6*52 variant.
rs28371733(G;G) is associated with: normal

743
-----------
My genotype at i4001467: GG or (G;G)
i4001467(A;A) is associated with: Homozygous for CYP2D6*4G non-functioning variant
i4001467(A;G) is associated with: Carrier of one CYP2D6*4G non-functioning variant
i4001467(G;G) is associated with: normal

744
-----------
My genotype at rs5030867: TT or (A;A)
rs5030867(A;A) is associated with: normal
rs5030867(A;C) is associated with: carrier of one CYP2D6*7 allele
rs5030867(C;C) is associated with: CYP2D6*7 homozygote

745
-----------
My genotype at i4001456: GG or (G;G)
i4001456(A;A) is associated with: Homozygous for CYP2D6*4F non-functioning variant
i4001456(A;G) is associated with: Carrier of one copy of CYP2D6*4F non-functioning variant.
i4001456(G;G) is associated with: normal

746
-----------
My genotype at rs1135824: TT or (A;A)
rs1135824(A;A) is associated with: normal
rs1135824(A;G) is associated with: One copy of CYP2D6*3B non-functioning variant.
rs1135824(G;G) is associated with: Two copies of CYP2D6*3B non-functioning variant

747
-----------
My genotype at rs28371706: GG or (C;C)
rs28371706(C;C) is associated with: normal
rs28371706(C;T) is associated with: Carrier of one CYP2D6 variant, possibly decreased on non-functioning.
rs28371706(T;T) is associated with: Homozygous for CYP2D6 variants, possibly decreased or non-functioning.

748
-----------
My genotype at i4001460: CC or (C;C)
i4001460(A;C) is associated with: common

749
-----------
My genotype at rs5030862: CC or (G;G)
rs5030862(A;A) is associated with: CYP2D6*12 homozygote
rs5030862(A;G) is associated with: carrier of one CYP2D6*12 allele
rs5030862(G;G) is associated with: normal

750
-----------
My genotype at rs4253623: AA or (A;A)
rs4253623(A;A) is associated with: normal
rs4253623(A;G) is associated with: 1.25x higher risk of nonfatal myocardial infarction
rs4253623(G;G) is associated with: 1.25x higher risk of nonfatal myocardial infarction

751
-----------
My genotype at rs5770917: TT or (T;T)
rs5770917(C;C) is associated with: >1.4x increased risk for narcolepsy
rs5770917(C;T) is associated with: 1.4x increased risk for narcolepsy
rs5770917(T;T) is associated with: normal

752
-----------
My genotype at rs4129148: GG or (G;G)
rs4129148(C;C) is associated with: >3x risk
rs4129148(C;G) is associated with: 3x risk
rs4129148(G;G) is associated with: common

753
-----------
My genotype at rs28694718: CC or (G;G)
rs28694718(A;A) is associated with: >2x risk
rs28694718(A;G) is associated with: 2x risk
rs28694718(G;G) is associated with: common