Chromosome 12
409 well-documented SNPs on chromosome 12, in order of position (GRCh38).
- rs11833579NINJ2 · 666,033A;ANo summary available.Typical
- rs12425791LOC105369597 · 674,318A;Apossibly increased risk of strokeTypical
- rs11554421WNK1 · 753,986G;Gcommon in clinvarTypical
- rs1012729WNK1 · 878,316A;AnormalTypical
- rs956868WNK1 · 881,746A;Acommon in clinvarTypical
- rs7955371WNK1 · 885,321C;Ccommon in complete genomicsTypical
- rs12828016WNK1 · 889,199G;Gcommon in clinvarTypical
- rs2270031WNT5B · 1,633,343C;Ccommon in complete genomicsTypical
- rs10848554ADIPOR2 · 1,696,421G;Gcommon in complete genomicsTypical
- rs767870ADIPOR2 · 1,780,657A;Acommon in complete genomicsTypical
- rs16928751ADIPOR2 · 1,781,033G;Gcommon in complete genomicsTypical
- rs1006737CACNA1C · 2,236,129A;Aincreased risk of Bipolar disorderMinor
- rs2159100CACNA1C · 2,237,227C;Ccommon/normalTypical
- rs1051375CACNA1C-AS1 · 2,679,713G;Gcommon in clinvarTypical
- rs42380104,009,151A;ANo summary available.Typical
- rs108490334,315,956A;Acommon in complete genomicsTypical
- rs11063112FGF23 · 4,368,914T;Tcommon in clinvarTypical
- rs7955866FGF23 · 4,370,383G;Gcommon in clinvarTypical
- rs193922702FGF23 · 4,370,563C;TAutosomal dominant hypophosphatemic rickets (predicted)Very important
- rs2970818C12orf4 · 4,497,002T;Tcommon on affy axiom dataTypical
- rs12302829FMR1NB · 5,031,318A;Acommon in complete genomicsTypical
- rs3741930KCNA5 · 5,043,981C;Ccommon in clinvarTypical
- rs45477792KCNA5 · 5,045,742C;CcommonTypical
- rs45438698KCNA5 · 5,045,880A;Anot seen (too rare)Typical
- rs1056468KCNA5 · 5,046,497A;Acommon in clinvarTypical
- rs2110166ANO2 · 5,642,176C;Ccommon genotypeTypical
- rs12579350ANO2 · 5,687,935G;Gcommon in complete genomicsTypical
- rs7962217VWF · 5,952,393C;Ccommon in clinvarTypical
- rs61750612VWF · 6,013,544A;AVon Willebrand disease, type 3Very important
- rs1800386VWF · 6,018,667C;Tassociation with Von Willebrand disease type 1Important
- rs216311VWF · 6,019,277T;Tcommon in clinvarTypical
- rs33978901VWF · 6,031,493C;Tassociation with Von Willebrand disease type 1Important
- rs216321VWF · 6,034,818C;Ccommon on affy axiom dataTypical
- rs62643632VWF · 6,044,298-;-Von Willebrand disease, type 3Very important
- rs1063857VWF · 6,044,348A;Acommon in clinvarTypical
- rs1063856VWF · 6,044,368T;Tcommon in clinvarTypical
- rs216293VWF · 6,044,493G;Gcommon in clinvarTypical
- rs1800378VWF · 6,063,036T;Tcommon in clinvarTypical
- rs7966230VWF · 6,126,464G;Gslightly lower levels of plasma VWFWorth knowing
- rs1800693TNFRSF1A · 6,330,843C;Cslight (1.4x) increase in risk for multiple sclerosisMinor
- rs4149639TNFRSF1A · 6,332,835T;Tcommon genotypeTypical
- rs4149584TNFRSF1A · 6,333,477C;Ccommon in clinvarTypical
- rs4149579TNFRSF1A · 6,338,191T;TTumor Necrosis Factor 1A Receptor Intron Variant HomozygousMinor
- rs767455TNFRSF1A · 6,341,779T;Tcommon in clinvarTypical
- rs2234649TNFRSF1A · 6,342,197T;Tcommon in complete genomicsTypical
- rs2228576SCNN1A · 6,347,896T;Tcommon in clinvarTypical
- rs5742912SCNN1A · 6,349,184A;Acommon in clinvarTypical
- rs4963516GNB3 · 6,838,864G;GNo summary available.Typical
- rs5442GNB3 · 6,845,700G;Gcommon in complete genomicsTypical
- rs5443GNB3 · 6,845,711T;Tviagra is more likely to have an effect. increased metabolic disease risk.Worth knowing
- rs7302230CLSTN3 · 7,135,836A;Acommon in complete genomicsTypical
- rs1805762M6PR · 8,945,306G;G>1.23x risk for hypertensionTypical
- rs669KLRG1 · 9,079,672C;C3.8x or higher increased risk for AlzheimersWorth knowing
- rs4763655KLRB1 · 9,602,982A;A>1.10x riskTypical
- rs11052552LOC105369652 · 9,703,362G;G1.4x risk of type-1 diabetesTypical
- rs16910526CLEC7A · 10,118,488C;CNo summary available.Important
- rs1050283OLR1 · 10,159,690G;Gincreased risk for Alzheimer'sTypical
- rs11053646OLR1 · 10,160,849C;Ccommon in complete genomicsTypical
- rs1049174KLRC4-KLRK1 · 10,372,766G;GnormalTypical
- rs2617170KLRC4 · 10,408,358C;CNormalTypical
- rs10772420TAS2R19 · 11,021,677A;AMore intense perception of quinineTypical
- rs2708377PRH1-TAS2R14 · 11,063,716T;TLess sensitive to bitter taste of CaffeineTypical
- rs2900174PRB2 · 11,394,598A;Acommon in complete genomicsTypical
- rs2160525LRP6 · 12,117,356G;Gcommon in complete genomicsTypical
- rs1012672LRP6 · 12,131,981G;Gcommon in complete genomicsTypical
- rs2302685LRP6 · 12,148,964T;Tcommon in complete genomicsTypical
- rs34330GPR19 · 12,717,761C;T1.3x higher risk for endometrial cancer (in Chinese women)Minor
- rs2066827GPR19 · 12,718,165T;Tcommon in clinvarTypical
- rs1805501GRIN2B · 13,561,125A;ANo summary available.Typical
- rs1805477GRIN2B · 13,561,795C;Ccommon in complete genomicsTypical
- rs890GRIN2B · 13,562,374A;Acommon in clinvarTypical
- rs1806201GRIN2B · 13,564,574G;Gcommon in clinvarTypical
- rs2160519GRIN2B · 13,634,912T;Tcommon on affy axiom dataTypical
- rs4764043GRIN2B · 13,962,548C;Ccommon in complete genomicsTypical
- rs11276ART4 · 14,840,505C;Ccommon in clinvarTypical
- rs4236MGP · 14,882,147T;Tcommon in clinvarTypical
- rs17415853EPS8 · 15,777,871T;Tcommon on affy axiom dataTypical
- rs296566717,291,799A;Aaspirin use may increase colorectal cancer risk a bitWorth knowing
- rs1050580617,335,830A;Acommon/normal; aspirin use reduces colorectal cancer risk a bitWorth knowing
- rs757326350PLCZ1 · 18,688,215A;AMale infertility (reported)Very important
- rs10770612LOC100506393 · 20,077,705A;Acommon in complete genomicsTypical
- rs11611208PDE3A · 20,605,679G;Gcommon on affy axiom dataTypical
- rs4149117SLCO1B3 · 20,858,546T;Tcommon in clinvarTypical
- rs7311358SLCO1B3 · 20,862,826G;Gcommon in clinvarTypical
- rs11045585SLCO1B3 · 20,892,760A;A24% chance (lower than average) of docetaxel-induced leukopenia/neutropeniaWorth knowing
- rs211703220,921,188C;Cincrease of 0.096 mg/dl in bilirubin levelsTypical
- rs4149013SLCO1B1 · 21,129,476A;Acommon in complete genomicsTypical
- rs4149018SLCO1B1 · 21,138,627T;Tcommon genotypeTypical
- rs7489119SLCO1B1 · 21,152,364C;Ccommon genotypeTypical
- rs2306283SLCO1B1 · 21,176,804A;Acommon in clinvarTypical
- rs11045818SLCO1B1 · 21,176,827G;Gcommon in clinvarTypical
- rs11045819SLCO1B1 · 21,176,879C;Ccommon on affy axiom dataTypical
- rs4149056SLCO1B1 · 21,178,615C;C17x myopathy risk for statin usersImportant
- rs2291075SLCO1B1 · 21,178,691C;Ccommon in clinvarTypical
- rs4363657SLCO1B1 · 21,215,788C;C17x increased myopathy risk for statin usersVery important
- rs11045879SLCO1B1 · 21,229,685T;Tcommon in clinvarTypical
- rs11568563SLCO1A2 · 21,304,500T;Tcommon in complete genomicsTypical
- rs11568564SLCO1A2 · 21,304,514G;Gcommon in complete genomicsTypical
- rs2306180GYS2 · 21,560,468T;Tcommon in clinvarTypical
- rs11046205ABCC9 · 21,839,392A;Arare genotype associated with longer sleep durationWorth knowing
- rs2900492ABCC9 · 21,889,314A;Acommon in complete genomicsTypical
- rs4762865ABCC9 · 21,925,372A;Acommon in complete genomicsTypical
- rs1074343021,998,639T;Tcommon in complete genomicsTypical
- rs1074346523,270,928G;Gcommon in complete genomicsTypical
- rs17287293LOC105369698 · 24,617,944A;Acommon on affy axiom dataTypical
- rs11047543LOC105369698 · 24,635,405G;Gcommon on affy axiom dataTypical
- rs7961152LOC105369699 · 24,828,677A;A1.5x higher risk for hypertensionWorth knowing
- rs12587KRAS · 25,205,894T;Tcommon in clinvarTypical
- rs9266KRAS · 25,209,283A;Acommon in clinvarTypical
- rs712KRAS · 25,209,618A;Acommon in clinvarTypical
- rs1137282KRAS · 25,209,843A;Acommon in clinvarTypical
- rs17388587KRAS · 25,236,286A;ANo summary available.Typical
- rs121912617BHLHE41 · 26,122,364C;CShort sleeperVery important
- rs16930692ITPR2 · 26,433,073A;ANo summary available.Typical
- rs2306677ITPR2 · 26,483,453G;GNo summary available.Typical
- rs1295KIAA1551 · 31,992,953G;Gcommon in complete genomicsTypical
- rs19129632,092,409G;Gcommon in complete genomicsTypical
- rs2630578BICD1 · 32,152,853G;Gcommon in complete genomicsTypical
- rs1151026BICD1 · 32,176,235A;Acommon in complete genomicsTypical
- rs11539445YARS2 · 32,755,303T;TMitochondrial respiratory chain (RC) disorder alleleVery important
- rs193922674PKP2 · 32,802,557C;GArrhythmogenic right ventricular dysplasiaVery important
- rs98357932,991,864G;GcommonTypical
- rs6582584ALG10B · 38,318,340G;Gcommon in complete genomicsTypical
- rs1994090SLC2A13 · 40,034,759G;GIncreased risk of developing Parkinson's DiseaseWorth knowing
- rs11175593LOC105369735 · 40,208,138C;Ccommon in complete genomicsTypical
- rs1491942LRRK2 · 40,227,006C;Ccommon in complete genomicsTypical
- rs34594498LRRK2 · 40,252,984C;TSlightly (~2x) higher risk of Parkinson's disease mutation, at least in Asians according to some studiesWorth knowing
- rs7308720LRRK2 · 40,263,898C;Ccommon in complete genomicsTypical
- rs7133914LRRK2 · 40,309,109G;Gcommon in complete genomicsTypical
- rs33939927LRRK2 · 40,310,434A;CParkinson's disease mutation, adult-onsetVery important
- rs11176013LRRK2 · 40,320,071A;Acommon in clinvarTypical
- rs11564148LRRK2 · 40,320,099T;Tcommon in clinvarTypical
- rs34637584LRRK2 · 40,340,400A;Apossible miscall in Ancestry V2.0 datasets; otherwise, 15 to 30% chance of Parkinson's disease, depending on age, family history, and ethnicityImportant
- rs33995883LRRK2 · 40,346,884A;GSlight (1.8x) increase in risk for Crohn's diseaseMinor
- rs3761863LOC105369736 · 40,364,850T;Tcommon in clinvarTypical
- rs11564258LOC105369736 · 40,398,498G;Gcommon in complete genomicsTypical
- rs13328933CNTN1 · 40,959,947C;Ccommon genotypeTypical
- rs1442190CNTN1 · 40,971,838G;Gcommon genotypeTypical
- rs1880887PDZRN4 · 41,327,628T;Tcommon in complete genomicsTypical
- rs285589PDZRN4 · 41,550,605T;Tcommon in complete genomicsTypical
- rs1796390PRICKLE1 · 42,484,802C;Ccommon/normalTypical
- rs152083242,859,612G;Gcommon in complete genomicsTypical
- rs4251424PUS7L · 43,760,023C;Ccommon genotypeTypical
- rs4251545IRAK4 · 43,786,492G;Gcommon in clinvarTypical
- rs1141168IRAK4 · 43,788,903A;Acommon in clinvarTypical
- rs17095830ANO6 · 45,381,125A;Acommon in complete genomicsTypical
- rs11610206LOC105369746 · 47,245,743T;Tcommon on affy axiom dataTypical
- rs11574129VDR · 47,843,520A;Acommon in clinvarTypical
- rs3847987VDR · 47,844,285C;Ccommon in clinvarTypical
- rs739837VDR · 47,844,438G;Gcommon in clinvarTypical
- rs731236VDR · 47,844,974A;GNo summary available.Typical
- rs1544410VDR · 47,846,052T;TIncreased risk of low bone mineral density disordersWorth knowing
- rs11574085VDR · 47,857,011T;Tcommon in complete genomicsTypical
- rs2107301VDR · 47,861,787A;A2.5x higher risk for prostate cancerImportant
- rs2228570VDR · 47,879,112A;Acommon in clinvarTypical
- rs4516035VDR · 47,906,043C;Cif less milk in teenage females, less bone?Typical
- rs2070739COL2A1 · 47,974,193G;GNo summary available.Typical
- rs1034762COL2A1 · 47,995,860C;CNo summary available.Typical
- rs3737548COL2A1 · 47,997,633G;Gcommon in clinvarTypical
- rs3803183COL2A1 · 48,004,297T;Tcommon in clinvarTypical
- rs17237198OR5BS1P · 48,560,149G;Gcommon on affy axiom dataTypical
- rs2070615CACNB3 · 48,824,388A;Gcommon in complete genomicsTypical
- rs3741559AQP2 · 49,951,193G;Gcommon in clinvarTypical
- rs467323AQP2 · 49,955,982C;Ccommon in clinvarTypical
- rs296766AQP2 · 49,957,170C;Ccommon in complete genomicsTypical
- rs3736309LOC101927318 · 49,964,271A;G0.44x decreased risk for chronic obstructive pulmonary lung diseaseWorth knowing
- rs17291650ATF1 · 50,819,650A;Acommon on affy axiom dataTypical
- rs12304921SLC11A2 · 50,963,759A;AnormalTypical
- rs1601012SCN8A · 51,685,722A;Apossible decreased suicide riskMinor
- rs60637SCN8A · 51,806,958C;Ccommon in clinvarTypical
- rs1712618051,870,172C;Ccommon in complete genomicsTypical
- rs2277382ACVRL1 · 51,912,437C;Ccommon in clinvarTypical
- rs2854464ACVR1B · 51,995,107A;Ahigher muscle strengthWorth knowing
- rs6580873KRT81 · 52,288,141C;Ccommon on affy axiom dataTypical
- rs2852464KRT83 · 52,316,937G;Gcommon in clinvarTypical
- rs61630004KRT85 · 52,367,173T;Tsignificance unclear; slight change related to ectodermal dysplasiaMinor
- rs641615KRT5 · 52,519,125G;Gcommon in clinvarTypical
- rs11170164KRT5 · 52,519,884T;T1.35x risk of basal cell carcinomaWorth knowing
- rs7959052KRT4 · 52,811,973T;Tcommon in clinvarTypical
- rs2638525KRT4 · 52,813,844G;Gcommon in clinvarTypical
- rs9658625SOAT2 · 53,103,618A;Acommon on affy axiom dataTypical
- rs2229774RARG · 53,211,761A;Ghigher risk for anthracycline side-effects for childhood cancer patientsImportant
- rs12321906ATF7 · 53,522,931T;Tcommon in complete genomicsTypical
- rs941184CALCOCO1 · 53,720,374C;Ccommon in complete genomicsTypical
- rs11614913MIR196A2 · 53,991,815C;CSomewhat increased risk of various types of cancerWorth knowing
- rs1800974ITGA7 · 55,695,573C;Tcommon in complete genomicsTypical
- rs17118154PMEL · 55,957,193C;GPossible mutation leading to pigment dispersion syndrome and pigmentary glaucomaVery important
- rs2069414CDK2 · 55,971,915C;CNo summary available.Typical
- rs17528736RAB5B · 55,974,734C;CNo summary available.Typical
- rs121908007SUOX · 56,004,039A;Asulfite oxidase deficiencyVery important
- rs10876864SUOX · 56,007,301A;AnormalTypical
- rs1131017LOC105369780 · 56,042,145C;Ccommon in clinvarTypical
- rs11171739ERBB3 · 56,076,841C;C1.75x risk of developing Type-1 diabetesWorth knowing
- rs2292239ERBB3 · 56,088,396T;T1.7x riskTypical
- rs11171806IL23A · 56,339,747G;Gcommon in clinvarTypical
- rs2066808STAT2 · 56,344,189A;ANo summary available.Typical
- rs2066807STAT2 · 56,346,898C;Ccommon in clinvarTypical
- rs11171846TIMELESS · 56,434,272C;CNo summary available.Typical
- rs11172113LRP1 · 57,133,500C;C0.8x lower risk for migrainesMinor
- rs1466535LRP1 · 57,140,687G;Gcommon/normalTypical
- rs1799986LRP1 · 57,141,483C;CNo summary available.Typical
- rs11544238ARHGAP9 · 57,476,372A;Acommon in clinvarTypical
- rs11547328CDK4 · 57,751,648G;Gcommon in complete genomicsTypical
- rs384293658,407,244C;TNo summary available.Typical
- rs7968324LOC100506869 · 58,672,798T;Tcommon genotypeTypical
- rs1117278258,865,846A;Acommon in complete genomicsTypical
- rs17121944LOC105369791 · 59,046,451T;Tcommon in complete genomicsTypical
- rs27600059,455,896C;Ccommon genotypeTypical
- rs730201762,610,803A;Acommon in complete genomicsTypical
- rs1050645863,051,312G;Gcommon on affy axiom dataTypical
- rs11174811AVPR1A · 63,146,696C;Ccommon in complete genomicsTypical
- rs10877969AVPR1A · 63,153,459T;Tcommon in complete genomicsTypical
- rs3759292AVPR1A · 63,153,533A;Acommon in complete genomicsTypical
- rs17120527RASSF3 · 64,622,520A;Acommon in complete genomicsTypical
- rs939876TBC1D30 · 64,858,338A;Acommon on affy axiom dataTypical
- rs17178006MSRB3 · 65,324,519T;Tcommon in complete genomicsTypical
- rs2272046HMGA2 · 65,830,681A;Acommon genotypeTypical
- rs10784502HMGA2 · 65,950,030C;Cbetter intracranial volume?Worth knowing
- rs1042725HMGA2 · 65,964,567C;C~0.8cm tallerMinor
- rs1117707468,150,654T;Tcommon in complete genomicsTypical
- rs1861494IFNG · 68,157,629C;TIBD riskMinor
- rs2069710IFNG · 68,159,895T;Tcommon in complete genomicsTypical
- rs2069709IFNG · 68,159,923C;Ccommon in complete genomicsTypical
- rs2069707IFNG · 68,160,508G;Gcommon in complete genomicsTypical
- rs318103268,162,395A;Acommon in complete genomicsTypical
- rs2870946LOC105369818 · 68,202,881T;Tcommon on affy axiom dataTypical
- rs416350TRAV8-6 · 68,385,633G;Gcommon in complete genomicsTypical
- rs2279744MDM2 · 68,808,800G;GGenerally more cancer proneWorth knowing
- rs315135YEATS4 · 69,369,207A;Acommon in complete genomicsTypical
- rs729761069,430,244C;Ccommon in clinvarTypical
- rs789560C12orf28 · 69,938,047G;Gcommon in complete genomicsTypical
- rs4489789PTPRR · 70,665,152T;Tcommon in complete genomicsTypical
- rs1705236TSPAN8 · 71,151,778T;Tcommon in complete genomicsTypical
- rs450056771,166,082G;Gcommon in complete genomicsTypical
- rs149537771,183,321G;GnormalTypical
- rs4570625TPH2 · 71,938,143G;Gmaybe: higher scores on anxiety-related personality traits; greater placebo responseMinor
- rs11178997TPH2 · 71,938,373T;TNo summary available.Typical
- rs4565946TPH2 · 71,942,989C;CRisk of early-onset OCDTypical
- rs1843809TPH2 · 71,954,918G;Gslightly decreased risk for ADHDMinor
- rs1386494TPH2 · 71,958,763A;GNo summary available.Typical
- rs17110563TPH2 · 71,972,526C;Ccommon in complete genomicsTypical
- rs7305115TPH2 · 71,979,082A;AIndividuals showed a significantly lower risk of suicide behavior than those with the A/G or G/G genotypeTypical
- rs11615016TPH2 · 72,022,214A;ANo summary available.Typical
- rs4290270TPH2 · 72,022,455A;Acommon in clinvarTypical
- rs17110747TPH2 · 72,032,174G;Gcommon in complete genomicsTypical
- rs12831974TRHDE · 72,330,254T;Tcommon in complete genomicsTypical
- rs1258265975,670,748T;Tcommon genotypeTypical
- rs1402279NAV3 · 77,335,605T;Tcommon on affy axiom dataTypical
- rs17005598SYT1 · 79,440,953G;Gcommon in complete genomicsTypical
- rs8176874PAWR · 79,620,593T;Tcommon in complete genomicsTypical
- rs17005769PAWR · 79,661,347T;Tcommon in complete genomicsTypical
- rs7297018PAWR · 79,668,450G;Gcommon on affy axiom dataTypical
- rs10506821RPL26P32 · 80,103,143C;Ccommon on affy axiom dataTypical
- rs28928909MYF6 · 80,708,053G;TPossible tendency for muscle cramps?Worth knowing
- rs1242513182,591,100G;Gcommon genotypeTypical
- rs11115322LOC107984487 · 82,625,409T;Tcommon genotypeTypical
- rs1545843LOC107984536 · 84,170,289A;A1.4x increased risk for depression (for those under 55)Minor
- rs103168184,526,555T;T1.3x increased risk for depression (for those under 55)Minor
- rs11836796CEP290 · 88,092,734T;Tcommon in complete genomicsTypical
- rs281865192CEP290 · 88,101,183C;CLeber Congenital Amaurosis (blindness)Very important
- rs995030KITLG · 88,496,894A;AReduced risk of testicular cancerWorth knowing
- rs3782179KITLG · 88,559,549C;C9x lower odds of testicular cancerWorth knowing
- rs4474514KITLG · 88,560,182A;A>3x increased testicular cancer risk for menMinor
- rs12821256KITLG · 88,934,558C;C4x more likely to have blond hairTypical
- rs1230252589,332,648C;Ccommon in complete genomicsTypical
- rs2681472ATP2B1 · 89,615,182A;ANo summary available.Typical
- rs2681492ATP2B1 · 89,619,312T;TNo summary available.Typical
- rs1847461LOC102724834 · 90,683,731G;Gcommon on affy axiom dataTypical
- rs2268578LUM · 91,107,421G;GnormalTypical
- rs3759223LUM · 91,113,006A;ANo summary available.Typical
- rs1701968291,911,494A;Acommon in complete genomicsTypical
- rs1021949592,496,744C;Ccommon on affy axiom dataTypical
- rs2289030KRT19P2 · 94,834,510G;Gcommon in complete genomicsTypical
- rs1085987195,318,100A;CSlight (~1.2x) increase in endometriosis riskMinor
- rs1110798795,330,153G;Gcommon in complete genomicsTypical
- rs713657295,566,012A;Acommon in complete genomicsTypical
- rs7297245HAL · 95,980,836C;Ccommon in clinvarTypical
- rs266086996,085,489G;Gcommon on affy axiom dataTypical
- rs1242324796,464,584A;Acommon genotypeTypical
- rs17028450TMPO · 98,534,325C;Ccommon in clinvarTypical
- rs7968606ANKS1B · 99,423,064C;Ccommon on affy axiom dataTypical
- rs11110077ANKS1B · 99,872,335C;Ccommon in complete genomicsTypical
- rs11110912LOC105369937 · 101,648,435C;GMaybe some quite minor increase in high blood pressure risk; data not replicated thoughTypical
- rs137853825GNPTAB · 101,753,376T;Tpossible association with stutteringWorth knowing
- rs137853823GNPTAB · 101,765,042C;Gpossible association with stutteringWorth knowing
- rs137853822GNPTAB · 101,768,082A;Cpossible association with stutteringWorth knowing
- rs7958709GNPTAB · 101,770,477T;Tcommon in clinvarTypical
- rs137853824GNPTAB · 101,770,558C;Tpossible association with stutteringWorth knowing
- rs2292303PARPBP · 102,119,753G;Gcommon in complete genomicsTypical
- rs1520223LOC105369942 · 102,332,560T;Tcommon in complete genomicsTypical
- rs5742714LOC105369942 · 102,396,074C;Ccommon in clinvarTypical
- rs6214LOC105369942 · 102,399,791C;Tcommon in complete genomicsTypical
- rs6218IGF1 · 102,399,855A;Acommon in clinvarTypical
- rs6220LOC105369942 · 102,400,737G;Gcommon in clinvarTypical
- rs5742692LOC105369942 · 102,405,820A;Acommon in complete genomicsTypical
- rs12423791IGF1 · 102,465,050G;Gcommon in complete genomicsTypical
- rs2288377IGF1 · 102,480,984A;Acommon in complete genomicsTypical
- rs5742612IGF1 · 102,481,086A;Acommon in complete genomicsTypical
- rs35767IGF1 · 102,481,791A;ANo summary available.Typical
- rs7965399LOC105369944 · 102,497,908T;Tcommon in complete genomicsTypical
- rs703556LOC105369944 · 102,618,116A;Acommon genotypeTypical
- rs5030860PAH · 102,840,474C;CHyperphenylalaninemia (non-phenylketonuria)Very important
- rs28934899PAH · 102,840,477G;GPhenyketonuriaVery important
- rs62642941PAH · 102,843,716-;-PhenylketonuriaVery important
- rs5030853PAH · 102,851,701A;APhenylketonuriaVery important
- rs5030849PAH · 102,852,875T;TPHENYLKETONURIA, MILDVery important
- rs1042503PAH · 102,852,922C;TBenign polymorphismMinor
- rs1718301PAH · 102,877,415G;Gcommon in clinvarTypical
- rs2037639PAH · 102,877,572G;Gcommon in clinvarTypical
- rs1522305PAH · 102,886,978C;CnormalTypical
- rs10860936PAH · 102,889,174T;Tcommon/normalTypical
- rs11111419PAH · 102,891,265A;Acommon/normalTypical
- rs62508727PAH · 102,894,801-;TCACarrier of a phenylketonuria mutationImportant
- rs4135150GLT8D2 · 103,989,821T;Tcommon in complete genomicsTypical
- rs6539137TXNRD1 · 104,313,402A;Aincreased risk for and earlier onset in males of familial ALSTypical
- rs4630362TXNRD1 · 104,333,966C;Ccommon in complete genomicsTypical
- rs12811699CHST11 · 104,623,386C;Ccommon in complete genomicsTypical
- rs2272495APPL2 · 105,190,099C;CNo summary available.Typical
- rs6539267POLR3B · 106,391,776C;CnormalTypical
- rs138249161POLR3B · 106,432,421A;AHypomyelinating leukodystrophy, type 8Very important
- rs3891355LOC100287944 · 106,556,917T;Tcommon on affy axiom dataTypical
- rs184039278CRY1 · 106,992,962G;GDelayed sleep phase possible; tendency to be a night owl?Important
- rs3794260LOC105369965 · 108,204,497A;A>1.26x risk for hypertensionTypical
- rs9739493WSCD2 · 108,250,412C;Chigher risk for hypertensionTypical
- rs918304108,483,764T;Tcommon genotypeTypical
- rs7300972SELPLG · 108,623,488T;Tcommon in complete genomicsTypical
- rs8179116LOC105369968 · 108,631,651C;Ccommon in complete genomicsTypical
- rs4623951DAO · 108,878,275T;Tcommon/normalTypical
- rs2070586DAO · 108,883,944G;Gcommon/normalTypical
- rs3741775DAO · 108,889,827A;Acommon/normalTypical
- rs3825251DAO · 108,894,208A;Acommon/normalTypical
- rs3219218UNG · 109,100,430A;Acommon in complete genomicsTypical
- rs9593MMAB · 109,557,065A;Acommon in clinvarTypical
- rs2287218MVK · 109,581,533T;TSlightly higher risk for CHD and ISWorth knowing
- rs3742030TRPV4 · 109,814,742G;Gcommon in complete genomicsTypical
- rs11065611110,266,682C;CNo summary available.Typical
- rs10774610CCDC63 · 110,902,439C;CLikely has alcohol flushTypical
- rs2188380110,948,323T;Tslightly higher risk for goutWorth knowing
- rs12229654110,976,657T;Tcommon in complete genomicsTypical
- rs3847953CUX2 · 111,327,660A;GNo summary available.Typical
- rs3184504SH2B3 · 111,446,804T;Tslightly (1.4x) increased risk for celiac diseaseMinor
- rs695871ATXN2 · 111,599,196G;Gcommon in clinvarTypical
- rs3782886BRAP · 111,672,685T;Tcommon in complete genomicsTypical
- rs659964ACAD10 · 111,692,395G;Gcommon in complete genomicsTypical
- rs11066015ACAD10 · 111,730,205G;Gcommon in complete genomicsTypical
- rs671ALDH2 · 111,803,962A;AAsian Flusher; increased risk of esophageal cancer; East Asian ancestry; Disulfiram not effective for alcoholism.Very important
- rs16941667ALDH2 · 111,806,609C;Ccommon in complete genomicsTypical
- rs17696736NAA25 · 112,049,014G;G1.94x risk of type-1 diabetesWorth knowing
- rs2074356C12orf51 · 112,207,597A;A2.2x increased risk for esophageal squamous cell cancer in Han ChineseWorth knowing
- rs11066280C12orf51 · 112,379,979T;Tcommon in complete genomicsTypical
- rs12229892PTPN11 · 112,485,589G;Gcommon in complete genomicsTypical
- rs3741981OAS1 · 112,911,065A;GNo summary available.Typical
- rs11066453OAS1 · 112,927,816A;Acommon in complete genomicsTypical
- rs12302655OAS3 · 112,936,701G;Gcommon in complete genomicsTypical
- rs2072134OAS3 · 112,971,371G;Gcommon in complete genomicsTypical
- rs7294372114,199,618T;Tcommon genotypeTypical
- rs569058293114,305,728C;Tfor heavy smokers, ~6x increased risk for COPDWorth knowing
- rs883079TBX5 · 114,355,435C;Ccommon in clinvarTypical
- rs11067600LOC105370003 · 115,439,972T;Tcommon in complete genomicsTypical
- rs17719439115,774,058G;Gcommon genotypeTypical
- rs2089222MAP1LC3B2 · 116,564,853G;Gcommon in complete genomicsTypical
- rs12322695RNFT2 · 116,761,609G;Gcommon genotypeTypical
- rs17429217HRK · 116,857,528A;Acommon genotypeTypical
- rs7294919116,889,787C;CEnhanced hippocampal volumeImportant
- rs3782206NOS1 · 117,307,284C;Ccommon in complete genomicsTypical
- rs10431397KSR2 · 117,668,389C;CNo summary available.Typical
- rs795484TAOK3 · 118,152,057T;TEven more increased morphine dose requirement and postoperative pain in tonsillectomy and adenoidectomyWorth knowing
- rs11613092118,455,443C;Ccommon in complete genomicsTypical
- rs11064768CCDC60 · 119,380,704A;Acommon on affy axiom dataTypical
- rs11064994BICDL1 · 120,017,960A;Acommon on affy axiom dataTypical
- rs17431357TRIAP1 · 120,442,631C;Ccommon genotypeTypical
- rs1799958ACADS · 120,738,280A;GConsidered to be a 'susceptibility' variant by some for SCAD; see textMinor
- rs3916ACADS · 120,739,469G;Gcommon in clinvarTypical
- rs1169300HNF1A · 120,993,422A;A~2x increased lung cancer riskWorth knowing
- rs2464196HNF1A · 120,997,624A;A~2x increased lung cancer riskWorth knowing
- rs1169305HNF1A · 120,999,579A;Gassociated with MODY3; maturity onset of diabetes in the young (type 3)Worth knowing
- rs1169310HNF1A · 121,001,630G;Gcommon in clinvarTypical
- rs7957197OASL · 121,022,883T;TNo summary available.Typical
- rs2230912P2RX7 · 121,184,393A;Acommon on affy axiom dataTypical
- rs3751143P2RX7 · 121,184,501A;Acommon in clinvarTypical
- rs3741595ORAI1 · 121,641,283C;Ccommon in clinvarTypical
- rs3741596ORAI1 · 121,641,389A;Acommon in complete genomicsTypical
- rs1154510LOC105370035 · 121,857,429C;Tlikely to be benignTypical
- rs3825172PSMD9 · 121,902,569C;Ccommon in complete genomicsTypical
- rs14259PSMD9 · 121,915,890A;Acommon in complete genomicsTypical
- rs7961894WDR66 · 121,927,677C;Ccommon in complete genomicsTypical
- rs830124WDR66 · 121,957,871G;Gcommon in complete genomicsTypical
- rs1316952DNAH10 · 123,915,003T;Tcommon in clinvarTypical
- rs9919713SCARB1 · 124,788,217A;Acommon in complete genomicsTypical
- rs74830677SCARB1 · 124,800,125A;Areported to be associated with higher HDL-CImportant
- rs5888SCARB1 · 124,800,202A;G3x higher risk for age-related macular degenerationWorth knowing
- rs4765623SCARB1 · 124,836,304C;Cmore likely to gain weight if taking olanzapineTypical
- rs1823172127,308,069C;Ccommon in complete genomicsTypical
- rs1075399TMEM132C · 128,463,014T;Tcommon in complete genomicsTypical
- rs1385374SLC15A4 · 128,816,149C;Ccommon on affy axiom dataTypical
- rs12580240TMEM132D · 129,162,027A;Acommon genotypeTypical
- rs12580533TMEM132D · 129,162,056T;Tcommon genotypeTypical
- rs1027557130,120,384C;Theterozygosity seems commonTypical
- rs1566667130,127,245A;ANo summary available.Typical
- rs11060845PIWIL1 · 130,367,629G;Gcommon in complete genomicsTypical
- rs11061269ADGRD1 · 130,971,904G;Gcommon genotypeTypical
- rs3847687ADGRD1 · 131,040,508C;Tcommon in complete genomicsTypical
- rs1569019ADGRD1 · 131,091,646C;Ccommon on affy axiom dataTypical
- rs10466868LOC101929974 · 131,455,375G;Gcommon on affy axiom dataTypical
- rs5744857POLE · 132,659,414C;Ccommon in clinvarTypical
- rs483352909POLE · 132,673,664C;GMuch higher risk for colorectal cancerVery important
- rs5744760POLE · 132,676,107C;TLikely benign variantMinor
- rs2306536CHFR · 132,847,076C;CaverageTypical
- rs2306541CHFR · 132,851,656G;GNo summary available.Typical
No matches.
Source and license
Adapted from SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.