Chromosome 11
545 well-documented SNPs on chromosome 11, in order of position (GRCh38).
- rs2280543BET1L · 203,788C;Ccommon in complete genomicsTypical
- rs12252IFITM3 · 320,772G;Gpossible miscall in Ancestry v2.0 datasets; otherwise, probably more susceptible to influenzaWorth knowing
- rs12628LRRC56 · 534,242A;Acommon in clinvarTypical
- rs4963128PHRF1 · 589,564C;Ccommon in complete genomicsTypical
- rs702966PHRF1 · 611,919C;Ccommon in complete genomicsTypical
- rs1061501IRF7 · 614,864T;Tcommon in complete genomicsTypical
- rs3758650CDHR5 · 616,865A;A6x increased risk for gallstone disease in Taiwanese/ChineseWorth knowing
- rs1800955DRD4 · 636,784C;Cincreased susceptibility to novelty seekingWorth knowing
- rs587776842DRD4 · 637,539-;-Autonomic nervous system dysfunction?Important
- rs1800443DRD4 · 639,830G;GRare DRD4 polymorphismImportant
- rs11246226DRD4 · 641,191A;Cdecreased risk of schizophrenia in limited studyMinor
- rs4331145DRD4 · 643,683T;Tincreased risk of schizophrenia in limited studyMinor
- rs11245936MUC2 · 1,086,366G;Gcommon on affy axiom dataTypical
- rs11245954MUC2 · 1,107,170A;Acommon on affy axiom dataTypical
- rs357059501,219,991T;TSignificantly higher (>10x) risk for lung issues (fibrosis or pneumonia)Very important
- rs5743867TOLLIP · 1,307,121A;Acommon in complete genomicsTypical
- rs17571CTSD · 1,761,364A;AIncrease in risk of vCJD. But rare.Worth knowing
- rs1003483IGF2 · 2,146,313G;TNo summary available.Typical
- rs4320932INS-IGF2 · 2,150,371C;C0.74x decreased risk for ovarian cancerMinor
- rs28933985INS · 2,159,919G;GNo summary available.Typical
- rs689INS · 2,160,994A;Acommon in clinvarTypical
- rs11042950TH · 2,168,488C;Ccommon in clinvarTypical
- rs6356TH · 2,169,721C;Ccommon in clinvarTypical
- rs2074238KCNQ1 · 2,463,573C;Ccommon on affy axiom dataTypical
- rs120074192KCNQ1 · 2,527,959A;GRomano-Ward Long QT SyndromeVery important
- rs120074177KCNQ1 · 2,570,682C;GRomano-Ward Long QT SyndromeVery important
- rs120074193KCNQ1 · 2,572,870A;GRomano-Ward Long QT SyndromeVery important
- rs120074194KCNQ1 · 2,572,871A;GRomano-Ward Long QT SyndromeVery important
- rs12720459KCNQ1 · 2,583,535C;TLQT1 form of Long QT syndromeVery important
- rs12720458KCNQ1 · 2,585,264A;Acommon in clinvarTypical
- rs17215500KCNQ1 · 2,768,881T;TLQT1 form of Long QT syndrome; Jervell and Lange-Nielsen syndromeVery important
- rs1057128KCNQ1 · 2,776,007G;Gcommon in clinvarTypical
- rs17221854KCNQ1 · 2,777,990T;Tincreased susceptibility to long QT syndromeVery important
- rs2074196KCNQ1 · 2,803,570G;Gcommon in complete genomicsTypical
- rs2237892KCNQ1 · 2,818,521C;Ccommon in complete genomicsTypical
- rs2283228KCNQ1 · 2,828,300A;Acommon in complete genomicsTypical
- rs2237897KCNQ1 · 2,837,316T;T1.4x increased risk for diabetic nephropathy in some populationsMinor
- rs1800172KCNQ1-AS1 · 2,847,899G;Gcommon in complete genomicsTypical
- rs8234KCNQ1-AS1 · 2,848,878A;Acommon in clinvarTypical
- rs10798KCNQ1-AS1 · 2,848,935A;Acommon in clinvarTypical
- rs16928809SLC22A18 · 2,915,722G;Gcommon on affy axiom dataTypical
- rs71203915,209,677T;Tcommon genotypeTypical
- rs34139813HBB · 5,225,657G;Ghomozygous Hb CreteImportant
- rs34690599HBB · 5,225,832C;CBeta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptomsVery important
- rs34451549HBB · 5,225,923A;ABeta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptomsVery important
- rs33915217HBB · 5,226,925C;GCarrier of a beta-thalassemia mutationImportant
- rs33956879HBB · 5,226,928A;Acommon in clinvarTypical
- rs33950507HBB · 5,226,943T;Treduction in malarial risk; mild anemiaVery important
- rs334HBB · 5,227,002A;Asickle cell anemiaVery important
- rs33930165HBB · 5,227,003T;T93% reduction in malarial riskTypical
- rs35848600HBD · 5,232,980G;Gcommon in complete genomicsTypical
- rs33956485HBD · 5,232,983A;Acommon in complete genomicsTypical
- rs35849348HBD · 5,232,998C;Ccommon in complete genomicsTypical
- rs33971270HBD · 5,233,059G;Gcommon in complete genomicsTypical
- rs34390965HBD · 5,233,991C;Ccommon in complete genomicsTypical
- rs35329985HBD · 5,234,008C;Ccommon in complete genomicsTypical
- rs35152987HBD · 5,234,352C;Ccommon in clinvarTypical
- rs34460332HBD · 5,234,360C;Ccommon in complete genomicsTypical
- rs35518301HBD · 5,234,514T;Tcommon in clinvarTypical
- rs34975911HBD · 5,234,560A;Acommon in clinvarTypical
- rs16912210HBBP1 · 5,242,623A;Acommon genotypeTypical
- i3003137HBB · 5,248,232A;ASickle Cell AnemiaVery important
- rs33947112HBG1 · 5,249,442C;Ccommon in complete genomicsTypical
- rs7482144HBG1 · 5,250,015G;Gcommon in clinvarTypical
- rs34807671HBG2 · 5,253,282G;Gcommon in complete genomicsTypical
- rs35481866HBG2 · 5,254,407T;Tcommon in complete genomicsTypical
- rs22131695,281,833G;Gcommon genotypeTypical
- rs49107425,285,279A;Acommon in complete genomicsTypical
- rs372091OR51B5 · 5,496,926G;Gcommon genotypeTypical
- rs3740996TRIM5 · 5,680,051G;Gcommon on affy axiom dataTypical
- rs1050239SMPD1 · 6,394,233G;Gcommon in clinvarTypical
- rs119455955TPP1 · 6,617,040A;ACLN2 disease (predicted)Very important
- rs56144125TPP1 · 6,617,154G;GCLN2 disease (predicted)Very important
- rs7107418OR10A2 · 6,871,595A;AMore likely to think cilantro tastes like soapWorth knowing
- rs11041530OVCH2 · 7,680,272G;Gcommon genotypeTypical
- rs12420464EIF3F · 7,993,230G;Gcommon on affy axiom dataTypical
- rs2272382TUB · 8,089,993T;Tslightly higher body mass indexTypical
- rs2272383TUB · 8,101,952A;Anormal riskTypical
- rs1528133RIC3 · 8,128,206T;Tnormal riskTypical
- rs110419LMO1 · 8,231,306A;A1.7x increased risk for neuroblastomaWorth knowing
- rs2168101LMO1 · 8,233,861C;Ccommon in clinvarTypical
- rs4910510LOC101928008 · 9,866,197T;Tcommon in complete genomicsTypical
- rs3814700ADM · 10,303,111T;Tcommon in complete genomicsTypical
- rs4910118ADM · 10,308,138C;Ccommon in complete genomicsTypical
- rs3741040AMPD3 · 10,500,245C;Ccommon in clinvarTypical
- rs7940423LOC107983976 · 11,482,681G;Gcommon in complete genomicsTypical
- rs3206824DKK3 · 11,964,514C;Ccommon in complete genomicsTypical
- rs7396187DKK3 · 11,967,604G;Gcommon in complete genomicsTypical
- rs2291599DKK3 · 11,968,352C;Ccommon in complete genomicsTypical
- rs16910421LOC105376554 · 12,049,118G;Gcommon genotypeTypical
- rs7120489PARVA · 12,447,850G;Gcommon in complete genomicsTypical
- rs11567847TEAD1 · 12,937,202T;Tcommon in clinvarTypical
- rs6256PTH · 13,492,506G;Gcommon in clinvarTypical
- rs11606345SPON1 · 14,197,151T;TNo summary available.Typical
- rs11023139SPON1 · 14,202,800G;Gcommon genotypeTypical
- rs117913124CYP2R1 · 14,879,385A;AAt least 2x higher risk for vitamin D insufficiency; also somewhat higher risk for MSImportant
- rs10741657LOC107984314 · 14,893,332G;Gtend to have lower vitamin D levelsMinor
- rs2060793LOC107984314 · 14,893,764A;ALower serum levels of vitamin DWorth knowing
- rs3781719CALCA · 14,972,978G;G2x increased hypertension riskTypical
- rs1102378715,930,748C;Ccommon in complete genomicsTypical
- rs4756846SOX6 · 16,381,965T;Tcommon on affy axiom dataTypical
- rs5215KCNJ11 · 17,387,083C;Ccommon in clinvarTypical
- rs1800467KCNJ11 · 17,387,284G;Gcommon in clinvarTypical
- rs80356616KCNJ11 · 17,387,917C;Ccommon in clinvarTypical
- rs5219KCNJ11 · 17,388,025T;T2.5x increased risk for type-2 diabetesWorth knowing
- rs137852676ABCC8 · 17,395,852C;Ccommon in clinvarTypical
- rs151344624ABCC8 · 17,395,889-;TTCCarrier of a hyperinsulinemic hypoglycemia mutationImportant
- rs757110ABCC8 · 17,396,930C;Ccommon in clinvarTypical
- rs151344623ABCC8 · 17,397,055C;TCarrier of a hyperinsulinemic hypoglycemia mutationImportant
- rs1048095ABCC8 · 17,461,731A;GReported to be associated with permanent neonatal diabetes mellitusVery important
- rs1064074USH1C · 17,498,195C;Ccommon in clinvarTypical
- rs1799913TPH1 · 18,025,708G;GHispanics may be at increased risk of heroin addiction.Minor
- rs12282742SAA2 · 18,244,252C;Ccommon in complete genomicsTypical
- rs3824886HTATIP2 · 20,383,067G;Gcommon in complete genomicsTypical
- rs7128311LOC645490 · 20,540,973T;Tcommon in complete genomicsTypical
- rs1443547SLC6A5 · 20,601,429G;Gcommon in clinvarTypical
- rs1443548SLC6A5 · 20,601,496T;Tcommon in clinvarTypical
- rs1793004NELL1 · 20,677,383G;Gincreased risk for Crohn's diseaseTypical
- rs8176785NELL1 · 20,783,740A;ANo summary available.Typical
- rs7481951ANO5 · 22,250,324A;Acommon in clinvarTypical
- rs1182796222,291,020C;CNo summary available.Typical
- rs711645623,933,767C;Ccommon genotypeTypical
- rs10500991LUZP2 · 24,828,020C;Ccommon on affy axiom dataTypical
- rs1279443525,186,158G;Gcommon in complete genomicsTypical
- rs6484176LOC105376596 · 25,766,084T;Tcommon in complete genomicsTypical
- rs12295638ANO3 · 26,583,784T;TNo summary available.Typical
- rs925946BDNFOS · 27,645,655G;Gcommon in complete genomicsTypical
- rs6265BDNF · 27,658,369T;Tintroversion; depression resistant; impaired motor skills learning; somewhat quicker mental decline in Alzheimer patientsWorth knowing
- rs8192466BDNF · 27,658,560A;AuncertainVery important
- rs12273539BDNF · 27,661,764C;Ccommon in complete genomicsTypical
- rs11030104BDNF · 27,662,970A;GNo summary available.Typical
- rs12291063BDNF · 27,672,554T;Tcommon genotypeTypical
- rs988748BDNF · 27,703,198C;GNo summary available.Typical
- rs90886727,724,217C;Ccommon in complete genomicsTypical
- rs160256529,140,589T;Tcommon on affy axiom dataTypical
- rs11031006LOC105376607 · 30,204,981A;Aslightly lower odds of giving birth to fraternal twinsMinor
- rs10835638FSHB · 30,230,805G;GcommonTypical
- rs3026398PAX6 · 31,787,227G;Gcommon in clinvarTypical
- rs662702PAX6 · 31,787,522C;Ccommon in clinvarTypical
- rs12421026PAX6 · 31,787,774C;Ccommon in clinvarTypical
- rs1506PAX6 · 31,788,750T;Tcommon in clinvarTypical
- rs644242PAX6 · 31,791,253C;CNo summary available.Typical
- rs667773PAX6 · 31,793,814G;Gcommon in clinvarTypical
- rs5030320WT1 · 32,388,456T;Tcommon in clinvarTypical
- rs5030317WT1 · 32,388,791C;Ccommon in clinvarTypical
- rs5030315WT1 · 32,388,970T;Tcommon in clinvarTypical
- rs1799937WT1 · 32,389,228A;Acommon in clinvarTypical
- rs28941779WT1 · 32,392,026A;GFrasier syndrome mutationVery important
- rs2234593WT1 · 32,392,787G;Gcommon in clinvarTypical
- rs16754WT1 · 32,396,399T;Tcommon in clinvarTypical
- rs10767942LOC101059934 · 32,500,461C;TNo summary available.Typical
- rs10437629C11orf41 · 33,566,664A;Acommon in complete genomicsTypical
- rs587777149CD59 · 33,717,393-;-inherited CD59 deficiencyVery important
- rs1103242333,847,061T;Tcommon genotypeTypical
- rs1001179CAT · 34,438,684T;T0.6x decreased acoustic neuroma riskTypical
- rs286913EHF · 34,633,816G;Gcommon in complete genomicsTypical
- rs2785173LOC100507144 · 35,134,185G;Gcommon in complete genomicsTypical
- rs187116CD44 · 35,144,253G;Gamong patients with gastric cancer, risk for more aggressive form?Minor
- rs369473842CD44 · 35,176,644C;CIN*B/B Indian Blood Group; possible donor of very rare blood typeVery important
- rs1467558CD44 · 35,208,126C;Ccommon on affy axiom dataTypical
- rs11821102CD44 · 35,230,997G;Gcommon in complete genomicsTypical
- rs13347CD44 · 35,231,725C;Ccommon in complete genomicsTypical
- rs7928794TRIM44 · 35,679,688A;Acommon in complete genomicsTypical
- rs3740955RAG1 · 36,574,050A;Acommon in clinvarTypical
- rs35691292RAG2 · 36,593,525G;Gcommon in clinvarTypical
- rs10836945LOC105376634 · 38,263,951C;Ccommon genotypeTypical
- rs11034653LOC105376634 · 38,267,043C;Ccommon genotypeTypical
- rs4611189LOC100507187 · 40,816,163G;Gcommon in complete genomicsTypical
- rs2862035LRRC4C · 41,203,883G;Gcommon genotypeTypical
- rs930003941,893,816A;Anormal riskTypical
- rs739457042,294,336G;Gcommon in complete genomicsTypical
- rs412960142,852,452A;Acommon genotypeTypical
- rs10501293RPL24 · 43,064,544T;TNo summary available.Typical
- rs1113132EXT2 · 44,231,853G;Gcommon in clinvarTypical
- rs11037909EXT2 · 44,234,064T;T1.47x type II diabetes riskMinor
- rs3740878EXT2 · 44,236,252T;T1.46x type II diabetes risk; commonMinor
- rs1103796544,356,606C;Ccommon genotypeTypical
- rs11038167TSPAN18 · 44,821,583A;Acommon in complete genomicsTypical
- rs2292912CRY2 · 45,856,137G;Gcommon in complete genomicsTypical
- rs10838527CRY2 · 45,881,643A;Acommon in complete genomicsTypical
- rs10742772PEX16 · 45,915,716T;Tcommon in complete genomicsTypical
- rs16938437PHF21A · 46,031,024C;Ccommon in complete genomicsTypical
- rs11038871DGKZ · 46,357,892T;Tcommon in complete genomicsTypical
- rs3136441F2 · 46,721,697T;Tcommon on affy axiom dataTypical
- rs2070852F2 · 46,723,375G;Gcommon in clinvarTypical
- rs5896F2 · 46,723,453C;Ccommon in clinvarTypical
- rs3136516F2 · 46,739,206G;Gcommon in clinvarTypical
- rs1799963F2 · 46,739,505A;A6.74x risk of thrombosis; 2-20x risk for cerebral stroke if PFO+Very important
- i300243246,761,055A;A6.7x increased risk of venous thromboembolismVery important
- rs2306029LRP4-AS1 · 46,871,557T;Tcommon in clinvarTypical
- rs2306033LRP4 · 46,875,895G;Gcommon on affy axiom dataTypical
- rs7117404C11orf49 · 47,105,602A;Acommon on affy axiom dataTypical
- rs747650C11orf49 · 47,154,454T;TLow risk of acne occurences in Chinese Han populationTypical
- rs1060573C11orf49 · 47,158,278T;TDecreased risk of acne occurrences in Chinese Han populationTypical
- rs4647707DDB2 · 47,215,017G;Gcommon in clinvarTypical
- rs2291120DDB2 · 47,216,129T;TNo summary available.Typical
- rs61731956NR1H3 · 47,268,596A;ANo summary available.Minor
- rs10501320LOC101928943 · 47,272,248G;Gcommon on affy axiom dataTypical
- rs121909377MYBPC3 · 47,333,238A;CMiscall likely if from 23andMe data; If not, familial hypertrophic cardiomyopathy 4Very important
- rs587782958MYBPC3 · 47,333,552C;TLikely miscall in 23andMe v5 data; otherwise, familial hypertrophic cardiomyopathy possibleVery important
- rs113358486MYBPC3 · 47,333,555A;CFamilial Hypertrophic CardiomyopathyVery important
- rs11570112MYBPC3 · 47,333,924C;Ginterpretation problematic vis-a-vis cardiomyopathy for several reasonsMinor
- rs2856655MYBPC3 · 47,337,534C;Ccommon in clinvarTypical
- rs397515963MYBPC3 · 47,337,729C;CLikely severe cardiomyopathyVery important
- rs111729952MYBPC3 · 47,337,796C;TFamilial Hypertrophic CardiomyopathyVery important
- rs181834806MYBPC3 · 47,342,658C;TConflicting Diagnosis for Hypertrophic CardiomyopathyWorth knowing
- rs375882485MYBPC3 · 47,342,698A;Gfamilial hypertrophic cardiomyopathy mutationVery important
- rs11570077MYBPC3 · 47,343,568G;Gcommon in clinvarTypical
- rs397516074MYBPC3 · 47,348,424C;Tfamilial hypertrophic cardiomyopathy mutationVery important
- rs11570045MYBPC3 · 47,351,323C;Ccommon in clinvarTypical
- rs376395543MYBPC3 · 47,351,507C;TFamilial Hypertrophic CardiomyopathyVery important
- rs45547231RAPSN · 47,448,165G;Gcommon in clinvarTypical
- rs4147730NDUFS3 · 47,583,875G;Gcommon/normalTypical
- rs1566734PTPRJ · 48,123,823C;Csomatic mutation found once in a colon cancerMinor
- rs1503185PTPRJ · 48,125,070C;CNo summary available.Typical
- rs5017948OR4A5 · 54,705,062T;Tcommon genotypeTypical
- rs7927370OR4A15 · 55,368,743C;Ccommon on affy axiom dataTypical
- rs2945816OR8I2 · 56,094,615T;Tcommon in complete genomicsTypical
- rs17150243OR5T3 · 56,252,449T;Tcommon genotypeTypical
- rs1122903057,435,536C;Chigher odds of Crohn's diseaseWorth knowing
- rs11546660SERPING1 · 57,599,994T;Tcommon in complete genomicsTypical
- rs11603020SERPING1 · 57,606,859T;Tcommon/normalTypical
- rs2511989SERPING1 · 57,610,852T;T0.44x decreased age-related macular degeneration riskWorth knowing
- rs2511988SERPING1 · 57,611,697A;Acommon in clinvarTypical
- rs4926SERPING1 · 57,614,516G;Gcommon in clinvarTypical
- rs8373ZFP91 · 58,610,951A;ANo summary available.Typical
- rs1800169ZFP91-CNTF · 58,624,028A;AnormalTypical
- rs250783858,705,326C;Ccommon genotypeTypical
- rs6591536OR5A1 · 59,443,715A;Aless able to detect β-ionone (floral) fragranceMinor
- rs558660GIF · 59,836,421G;Gcommon/normalTypical
- rs526934TCN1 · 59,866,020A;Acommon/normalTypical
- rs2298585MS4A3 · 60,069,719C;Ccommon in complete genomicsTypical
- rs574700MS4A2 · 60,088,010C;Ccommon in complete genomicsTypical
- rs569108MS4A2 · 60,095,631T;TNo summary available.Typical
- rs512555MS4A2 · 60,095,780C;CNo summary available.Typical
- rs610932MS4A6A · 60,171,834T;TA allele associated with reduced risk of Alzheimer's in Chinese Han population.Minor
- rs670139MS4A4E · 60,204,322G;Gcommon/normalTypical
- rs17824933CD6 · 60,993,140C;Ccommon on affy axiom dataTypical
- rs174537MYRF · 61,785,208T;Tlower LDL-C and total cholesterolWorth knowing
- rs7102974FEN1 · 61,792,563C;CNo summary available.Typical
- rs174548FADS1 · 61,803,876C;Chighest phosphatidylcholine valuesTypical
- rs174570FADS2 · 61,829,740C;CNo summary available.Typical
- rs1535FADS2 · 61,830,500A;ANo summary available.Typical
- rs174575FADS2 · 61,834,531C;CNo summary available.Typical
- rs66698963FADS2 · 61,835,065CTCCCTGCCTCCCCAGGGACTT;CTCCCTGCCTCCCCAGGGACTTcommon in clinvarTypical
- rs482548FADS2 · 61,865,710C;CNo summary available.Typical
- rs2521572RAB3IL1 · 61,944,003G;Gcommon in complete genomicsTypical
- rs1109748BEST1 · 61,955,173C;Ccommon in clinvarTypical
- rs1123087462,028,114T;Tcommon in complete genomicsTypical
- rs137852971HNRNPUL2-BSCL2 · 62,692,413G;GCongenital generalized lipodystrophy, type 2Very important
- rs35730843POLR2G · 62,760,162A;Acommon genotypeTypical
- rs2186410CHRM1 · 62,917,945G;GNo summary available.Typical
- rs11568634SLC22A6 · 62,979,488C;Ccommon in complete genomicsTypical
- rs11568482SLC22A8 · 62,995,792T;Tcommon in complete genomicsTypical
- rs11568492SLC22A8 · 62,996,085G;Gcommon in complete genomicsTypical
- rs11568493SLC22A8 · 62,996,135A;Acommon in complete genomicsTypical
- rs4980524STIP1 · 64,191,787C;CNo summary available.Typical
- rs12800450SLC22A12 · 64,591,749G;Gcommon in complete genomicsTypical
- rs11231825SLC22A12 · 64,592,802T;Tcommon in clinvarTypical
- rs7932775SLC22A12 · 64,600,390T;Tcommon in clinvarTypical
- rs589691PYGM · 64,757,744C;Ccommon in clinvarTypical
- rs493573MAP4K2 · 64,789,582C;Ccommon in complete genomicsTypical
- rs2959656MEN1 · 64,804,546T;Tcommon in clinvarTypical
- rs11231898MIR194-2HG · 64,891,364G;Gcommon in complete genomicsTypical
- rs487989POLA2 · 65,297,219G;Gcommon on affy axiom dataTypical
- rs619586MALAT1 · 65,498,698A;Acommon genotypeTypical
- rs7927113MALAT1 · 65,500,727G;Gcommon genotypeTypical
- rs3782089SSSCA1 · 65,569,348C;Ccommon in complete genomicsTypical
- rs931127SIPA1 · 65,637,829A;A2.15x more likely positive lymph nodeWorth knowing
- rs2448490SIPA1 · 65,644,564A;A0.57x (reduced) risk for metastasis in LN-/ER+ breast cancer patientsTypical
- rs1893316CATSPER1 · 66,026,326G;Gcommon in clinvarTypical
- rs4073582CNIH2 · 66,283,241A;Alower risk for goutWorth knowing
- rs35520756BBS1 · 66,519,725G;Gcommon in clinvarTypical
- rs1815739ACTN3 · 66,560,624C;CBetter performing muscles. Likely sprinter.Worth knowing
- rs2228325ACTN3 · 66,560,624T;Timpaired muscle performanceWorth knowing
- rs28940591PC · 66,871,368A;Acommon in clinvarTypical
- rs1894111GRK2 · 67,271,141C;Ccommon in complete genomicsTypical
- rs8191439GSTP1 · 67,583,826G;Gcommon in complete genomicsTypical
- rs1695GSTP1 · 67,585,218G;G3.5x asthma risk in certain populationsWorth knowing
- rs749174GSTP1 · 67,585,782G;Gcommon in complete genomicsTypical
- rs1138272GSTP1 · 67,586,108C;Ccommon in complete genomicsTypical
- rs1871042GSTP1 · 67,586,373C;Ccommon in complete genomicsTypical
- rs947895GSTP1 · 67,586,935C;Ccommon in complete genomicsTypical
- rs4988300LRP5 · 68,321,363G;TNo summary available.Typical
- rs4988321LRP5 · 68,406,721A;Aslightly increased (~1.3x) risk for osteoporosisMinor
- rs2306862LRP5 · 68,410,042C;Ccommon in clinvarTypical
- rs3736228LRP5 · 68,433,827T;Tincreased risk for osteoporosisMinor
- rs694066LOC107984343 · 68,685,517G;Gcommon in complete genomicsTypical
- rs2229738CPT1A · 68,794,860C;Ccommon in clinvarTypical
- rs560096IGHMBP2 · 68,911,494T;Tcommon in clinvarTypical
- rs10896380IGHMBP2 · 68,914,934A;Acommon in clinvarTypical
- rs622082IGHMBP2 · 68,936,491A;Acommon in clinvarTypical
- rs35264875TPCN2 · 69,078,931T;Tblonde hair colorImportant
- rs3829241TPCN2 · 69,087,895G;Gcommon in clinvarTypical
- rs1279375969,207,088G;Gcommon in complete genomicsTypical
- rs7130881LOC105369367 · 69,228,491A;Acommon in complete genomicsTypical
- rs7105934LOC102724265 · 69,424,973A;A0.48 times lower odds of developing renal cell carcinomaWorth knowing
- rs603965CCND1 · 69,648,142A;AnormalTypical
- rs80338859DHCR7 · 71,435,827A;AMiscall for 23andMe customers; otherwise, Smith-Lemli-Opitz syndromeVery important
- rs11555217DHCR7 · 71,441,401C;TUnaffected carrier of a Smith-Lemli-Opitz syndrome mutationImportant
- rs12785878NADSYN1 · 71,456,403T;Tslightly increased (1.4x) risk for vitamin D insufficiencyMinor
- rs7925545FOLR3 · 72,134,495A;Acommon in complete genomicsTypical
- rs7926875FOLR3 · 72,138,396C;Ccommon in complete genomicsTypical
- rs7926987FOLR3 · 72,138,457C;Ccommon in complete genomicsTypical
- rs2071010FOLR1 · 72,189,920G;Gcommon/normalTypical
- rs655423INPPL1 · 72,234,616G;Gcommon in clinvarTypical
- rs1241820472,539,079G;Gcommon on affy axiom dataTypical
- rs11603334ARAP1 · 72,721,940G;Gcommon on affy axiom dataTypical
- rs1123566773,152,652A;Acommon genotypeTypical
- rs660339UCP2 · 73,978,059G;Gcommon in clinvarTypical
- rs2075577UCP3 · 74,004,497G;GLarger stomach volume, does not get full as easily as T allele carriersWorth knowing
- rs2229707UCP3 · 74,006,202C;Ccommon in complete genomicsTypical
- rs2734830UCP3 · 74,006,202C;CNo summary available.Typical
- rs2270676KCNE3 · 74,457,366A;Acommon in complete genomicsTypical
- rs2306168SLCO2B1 · 75,196,537C;Ccommon in complete genomicsTypical
- rs472112ARRB1 · 75,310,457C;Tcommon in complete genomicsTypical
- rs634552SERPINH1 · 75,571,007T;TAMD AssociationMinor
- rs1458836UVRAG · 75,813,751C;Ccommon in complete genomicsTypical
- rs7933235UVRAG · 75,829,541A;Acommon in complete genomicsTypical
- rs215521976,588,150T;TNo summary available.Typical
- rs792789476,590,272C;C0.83x lower risk of Atopic Dermatitis.Worth knowing
- rs3781684CAPN5 · 77,112,438C;Ccommon in complete genomicsTypical
- rs1052030MYO7A · 77,142,737A;TCarrier of a mutation for deafnessImportant
- rs139889944MYO7A · 77,199,771G;Gcommon in clinvarTypical
- rs948962MYO7A · 77,208,433C;Ccommon in clinvarTypical
- rs527589PAK1 · 77,443,594T;Tcommon in complete genomicsTypical
- rs7101429GAB2 · 78,281,921G;G0.70x reduced risk for Alzheimer's riskWorth knowing
- rs2373115GAB2 · 78,380,104C;CNo summary available.Typical
- rs11232369LOC101928964 · 80,851,695G;Gcommon genotypeTypical
- rs135733981,143,332C;Ccommon on affy axiom dataTypical
- rs145809581,274,505C;Ccommon in complete genomicsTypical
- rs2298668PRCP · 82,853,252T;Tcommon in complete genomicsTypical
- rs3885683DLG2 · 83,744,664T;Tcommon in complete genomicsTypical
- rs10501570DLG2 · 84,706,803T;TNormal risk of developing Parkinson's DiseaseMinor
- rs17148090DLG2 · 85,306,432A;Acommon in complete genomicsTypical
- rs592297PICALM · 86,014,894C;Ccommon in clinvarTypical
- rs385117986,157,598T;T0.85x decreased risk for Alzheimer's diseaseMinor
- rs2015747PRSS23 · 86,792,095C;Ccommon in complete genomicsTypical
- rs713065PRSS23 · 86,946,478A;Acommon in clinvarTypical
- rs10898563PRSS23 · 86,948,171A;Acommon in clinvarTypical
- rs1386330RAB38 · 88,086,259T;Tcommon in complete genomicsTypical
- rs217116CTSC · 88,300,493A;Acommon in clinvarTypical
- rs217086CTSC · 88,312,415A;Acommon in clinvarTypical
- rs16914280GRM5 · 88,588,556C;Ccommon in complete genomicsTypical
- rs1799989TYR · 89,177,755A;Cbenign most likelyTypical
- rs1042602TYR · 89,178,528A;Aassociated with the absence of frecklesTypical
- rs1393350TYR · 89,277,878A;ANo summary available.Important
- rs1126809TYR · 89,284,793A;Aslight increase in skin cancer riskTypical
- rs1800422TYR · 89,284,793G;GNo summary available.Typical
- rs12274302DISC1FP1 · 90,853,732C;Ccommon in complete genomicsTypical
- rs7950811MIR194-2 · 92,917,836C;Ccommon in complete genomicsTypical
- rs10830963MTNR1B · 92,975,544G;Gincreased type-2 diabetes risk; higher gestational diabetes riskImportant
- rs3781637MTNR1B · 92,980,604T;Tcommon in complete genomicsTypical
- rs7931462RPL26P31 · 93,051,037G;GNo summary available.Typical
- rs1182570993,970,883A;Acommon genotypeTypical
- rs11020790MRE11A · 94,466,544C;Ccommon in complete genomicsTypical
- rs13447640MRE11 · 94,466,555G;Gcommon in complete genomicsTypical
- rs1805363MRE11A · 94,493,786C;Ccommon in clinvarTypical
- rs1083128494,934,799A;ANo summary available.Typical
- rs10765792MAML2 · 96,133,536G;Gcommon on affy axiom dataTypical
- rs1122489997,088,525G;Gcommon genotypeTypical
- rs1121236497,703,984A;Acommon in complete genomicsTypical
- rs1121722398,852,486A;Acommon genotypeTypical
- rs10501920CNTN5 · 99,622,442C;Ccommon in complete genomicsTypical
- rs12803066CNTN5 · 100,172,688A;Gincreased risk of myopiaWorth knowing
- rs11223581CNTN5 · 100,302,805A;Acommon genotypeTypical
- rs12800752100,535,909T;Tcommon genotypeTypical
- rs471767PGR · 101,034,566A;GNo summary available.Typical
- rs500760PGR · 101,039,260C;CNo summary available.Typical
- rs1042838PGR · 101,062,681A;A1.42x risk for endometrial ovarian cancer; overlaps with rs608995Important
- rs503362PGR · 101,091,096C;GNo summary available.Typical
- rs10895068PGR · 101,129,483T;T2.5x increased odds of breast cancer among hormone-using postmenopausal womenMinor
- rs12366144TRPC6 · 101,476,362A;Acommon in clinvarTypical
- rs11225148YAP1 · 102,138,549A;ANo summary available.Typical
- rs2852894102,284,743G;Gcommon in complete genomicsTypical
- rs11225297102,517,147A;ANo summary available.Typical
- rs12184413MMP7 · 102,518,857C;CnormalTypical
- rs1711437MMP20 · 102,594,495C;Cslightly reduced creatinine clearanceWorth knowing
- rs10895322MMP20 · 102,599,525A;Acommon in clinvarTypical
- rs1940475MMP8 · 102,722,517T;Tcommon in clinvarTypical
- rs17099545LOC100128088 · 102,761,462A;Acommon in complete genomicsTypical
- rs486055MMP10 · 102,779,693C;Ccommon on affy axiom dataTypical
- rs10488MMP1 · 102,797,291C;Ccommon in clinvarTypical
- rs1144393MMP1 · 102,798,678C;C1.3x risk of chronic kidney disease in JapaneseTypical
- rs2075847MMP1 · 102,799,093A;Acommon in complete genomicsTypical
- rs1799750MMP1 · 102,799,765C;Cin breast cancer patients, slightly higher risk for poorer prognosisMinor
- rs569444WTAPP1 · 102,836,574G;Gcommon in complete genomicsTypical
- rs650108MMP3 · 102,838,056A;Ahigher risk for Achilles tendinopathy?Minor
- rs591058MMP3 · 102,840,607C;Chigher risk for Achilles tendinopathy?Minor
- rs679620MMP3 · 102,842,889C;Chigher risk for Achilles tendinopathy?Minor
- rs3025058MMP3 · 102,845,217-;-5A/5A; higher MI risk?Typical
- rs610950102,848,999T;Tcommon in complete genomicsTypical
- rs652438MMP12 · 102,865,911T;Tcommon in complete genomicsTypical
- rs17368582MMP12 · 102,867,344T;Tcommon in complete genomicsTypical
- rs2276109MMP12 · 102,875,061T;Tcommon in complete genomicsTypical
- rs1277718MMP12 · 102,876,821G;Gcommon in complete genomicsTypical
- rs3819089MMP13 · 102,952,004C;Ccommon in clinvarTypical
- rs7947821DCUN1D5 · 103,076,736T;Tcommon genotypeTypical
- rs12283022DYNC2H1 · 103,109,865A;Acommon genotypeTypical
- rs12294076DYNC2H1 · 103,256,336T;Tcommon genotypeTypical
- rs716274103,547,430A;Acommon in clinvarTypical
- rs1917445103,718,366C;Tcommon in complete genomicsTypical
- rs11226373104,463,511A;Acommon in complete genomicsTypical
- rs497116CASP12 · 104,892,390A;Acommon in complete genomicsTypical
- rs556205CASP1 · 105,027,281T;TNo summary available.Typical
- rs7937106107,483,586T;Tcommon genotypeTypical
- rs10502094ALKBH8 · 107,559,328A;Acommon in complete genomicsTypical
- rs3741049ACAT1 · 108,139,200G;GNo summary available.Typical
- rs1800054ATM · 108,227,849G;G1.5x increased risk for breast cancerMinor
- rs3218707ATM · 108,244,000G;Gcommon in complete genomicsTypical
- rs2227924ATM · 108,251,865C;Ccommon in complete genomicsTypical
- rs4986761ATM · 108,254,034C;Cvery slightly increased (1.5x or less) breast cancer riskMinor
- rs3218695ATM · 108,259,051C;Ccommon in complete genomicsTypical
- rs1800056ATM · 108,267,276C;Cvery slightly increased (1.5x or less) breast cancer riskMinor
- rs664677ATM · 108,272,455C;CLower lung cancer and increased breast cancer riskWorth knowing
- rs3092857ATM · 108,272,572A;Acommon in complete genomicsTypical
- rs1800057ATM · 108,272,729G;Gvery slightly increased breast cancer riskMinor
- rs3092856ATM · 108,289,005C;Ccommon in complete genomicsTypical
- rs1800058ATM · 108,289,623T;T1.5x increased risk for breast cancerMinor
- rs1801516ATM · 108,304,735A;A2.76x odds of pancreatic cancer, but 0.86x reduced risk of melanomaWorth knowing
- rs1801673ATM · 108,304,736A;Acommon in complete genomicsTypical
- rs659243C11orf65 · 108,312,440A;Acommon in clinvarTypical
- rs28904921C11orf65 · 108,329,202G;T~8 fold increase in relative risk for breast cancerVery important
- rs664143ATM · 108,354,934A;GHigher risk for number of cancersWorth knowing
- rs227092ATM · 108,366,056G;Gcommon in clinvarTypical
- rs3092844C11orf65 · 108,368,580C;Ccommon in complete genomicsTypical
- rs4585ATM · 108,368,901G;Gslightly higher (1.35x) odds of good metformin response in type 2 diabeticsWorth knowing
- rs11212617C11orf65 · 108,412,434A;CSomewhat increased likelihood of treatment success with metforminMinor
- rs11213809C11orf53 · 111,265,020G;Gcommon/normalTypical
- rs3802842COLCA2 · 111,300,984C;C>1.17x increased risk of colorectal cancerWorth knowing
- rs2303436DLAT · 112,025,600A;GNo summary available.Typical
- rs627441DLAT · 112,037,438T;Tcommon in clinvarTypical
- rs34677591SDHD · 112,086,941A;Geither just a polymorphism, or, a slight cancer predisposing mutationWorth knowing
- rs1834481IL18 · 112,153,104C;Ccommon on affy axiom dataTypical
- rs5744247IL18 · 112,155,433G;Gcommon in complete genomicsTypical
- rs5744241IL18 · 112,156,421T;Tcommon in complete genomicsTypical
- rs187238IL18 · 112,164,265C;Chypertension increases risk 3.75x for sudden cardiac deathWorth knowing
- rs7105056BCO2 · 112,193,708C;CNo summary available.Typical
- rs3819331PTS · 112,228,687C;Cincreased risk of autismWorth knowing
- rs1436109NCAM1 · 113,120,896G;Gcommon on affy axiom dataTypical
- rs11604671ANKK1 · 113,397,337G;Gcommon/normalTypical
- rs4938016ANKK1 · 113,399,293C;Ccommon/normalTypical
- rs2734849ANKK1 · 113,399,438A;Acommon/normalTypical
- rs2734848ANKK1 · 113,399,652T;Tcommon/normalTypical
- rs1800497ANKK1 · 113,400,106A;AA1/A1: Bad at avoidance of errors. 0.25x lower OCD; 0.56x lower Tardive Diskinesia; higher ADHD; 1.4x Alcohol Dependence; lower Postoperative Nausea; Increased obesity; less pleasure response; Bupropion ineffective for smoking cessation.; 2.4x risk for adenoma recurrence.Very important
- rs6277DRD2 · 113,412,737A;Anormal schizophrenia risk, learns NoGo fasterWorth knowing
- rs6275DRD2 · 113,412,755A;Acommon in clinvarTypical
- rs1801028DRD2 · 113,412,762G;Gnormal riskTypical
- rs1800496DRD2 · 113,412,766G;Gcommon in complete genomicsTypical
- rs1076560DRD2 · 113,412,966A;Ainfluences working memoryWorth knowing
- rs11214606DRD2 · 113,439,147C;Ccommon on affy axiom dataTypical
- rs4648317DRD2 · 113,460,810A;Aprone to higher nicotine dependence, more impulsive/sensation seekingMinor
- rs11214613DRD2 · 113,464,537G;Gcommon in complete genomicsTypical
- rs1799732DRD2 · 113,475,529-;-less favorable clinical outcome when on antipsychoticsWorth knowing
- rs1799978DRD2 · 113,475,629T;Tcommon in clinvarTypical
- rs12364283DRD2 · 113,476,233A;Acommon in complete genomicsTypical
- rs11606194HTR3B · 113,910,259T;TNo summary available.Typical
- rs2276307HTR3B · 113,933,165A;ANo summary available.Typical
- rs1150226HTR3A · 113,974,819G;Gcommon in complete genomicsTypical
- rs11608105CADM1 · 115,380,472C;Ccommon genotypeTypical
- rs11215936LOC107987166 · 116,442,799G;Gcommon in complete genomicsTypical
- rs7350481116,715,567C;Ccommon on affy axiom dataTypical
- rs12272004116,733,008C;CNo summary available.Typical
- rs1558861116,736,721T;Tcommon on affy axiom dataTypical
- rs11216126BUD13 · 116,746,524A;Acommon in complete genomicsTypical
- rs11825181BUD13 · 116,755,542G;GNo summary available.Typical
- rs11820589BUD13 · 116,763,146G;GNo summary available.Typical
- rs10790162BUD13 · 116,768,388G;Gcommon on affy axiom dataTypical
- rs964184ZNF259 · 116,778,201G;Gincreased risk of hypertriglyceridemiaWorth knowing
- rs11823543ZNF259 · 116,778,419G;GNo summary available.Typical
- rs12286037ZNF259 · 116,781,491C;CNo summary available.Typical
- rs6589566ZNF259 · 116,781,707A;Acommon on affy axiom dataTypical
- rs2266788ZPR1 · 116,789,970A;Acommon on affy axiom dataTypical
- rs2075291ZPR1 · 116,790,676C;CnormalTypical
- rs3135506APOA5 · 116,791,691G;Gcommon on affy axiom dataTypical
- rs662799APOA5 · 116,792,991A;G1.4x higher early heart attack risk; less weight gain on high fat dietsWorth knowing
- rs633389116,796,621C;Ccommon genotypeTypical
- rs5110APOA4 · 116,820,918C;Ccommon in clinvarTypical
- rs2542052APOC3 · 116,829,268A;ANormal (Reference)Worth knowing
- rs76353203APOC3 · 116,830,637C;Trare variant with large positive effectVery important
- rs138326449APOC3 · 116,830,638A;Grare variant with large positive effectVery important
- rs147210663APOC3 · 116,830,844A;Grare variant with large positive effectVery important
- rs11216185SIK3 · 116,912,258T;Tcommon in complete genomicsTypical
- rs508487TAGLN · 117,204,850C;Ccommon in complete genomicsTypical
- rs1047964BACE1 · 117,286,177G;Gcommon on affy axiom dataTypical
- rs638405BACE1 · 117,293,108G;G2x increased ALZ risk in ApoE4 carriersWorth knowing
- rs10892151DSCAML1 · 117,661,016C;Ccommon in complete genomicsTypical
- rs3135932IL10RA · 117,993,348A;Acommon on affy axiom dataTypical
- rs2228054IL10RA · 117,993,398G;Gcommon in clinvarTypical
- rs2228055IL10RA · 117,994,131A;Acommon in clinvarTypical
- rs4252314IL10RA · 117,997,802A;ANo summary available.Typical
- rs9610IL10RA · 118,001,371G;Gcommon in clinvarTypical
- rs11216831MPZL3 · 118,246,303G;GNo summary available.Typical
- rs1784246KMT2A · 118,480,197A;Acommon in complete genomicsTypical
- rs498872PHLDB1 · 118,606,652A;A1.4x higher risk for glioma developmentMinor
- rs638893118,827,828G;G1.22x risk of vitiligo in ChineseTypical
- rs6421571118,873,063C;Ccommon in complete genomicsTypical
- rs630923CXCR5 · 118,883,644C;Ccommon in complete genomicsTypical
- rs80356489SLC37A4 · 119,028,223G;Gglycogen storage disease type 1b disease alleleVery important
- rs7759DPAGT1 · 119,096,581A;Acommon in clinvarTypical
- rs643788DPAGT1 · 119,097,048T;Tcommon in clinvarTypical
- rs587776596MFRP · 119,345,563-;GCarrier of a microphthalmia mutationImportant
- rs1954787GRIK4 · 120,792,654T;T~10% less likely to respond to citalopramWorth knowing
- rs12797755GRIK4 · 120,938,751T;Tcommon on affy axiom dataTypical
- rs7946599SORL1 · 121,552,931G;Gcommon in complete genomicsTypical
- rs2298814SORL1 · 121,554,173G;Gcommon in complete genomicsTypical
- rs6589885SORL1 · 121,555,333G;Gcommon in complete genomicsTypical
- rs720099SORL1 · 121,563,084T;Tcommon in complete genomicsTypical
- rs11218342SORL1 · 121,563,719T;Tcommon in complete genomicsTypical
- rs11218343SORL1 · 121,564,878T;TNo summary available.Typical
- rs1784919SORL1 · 121,568,956C;Ccommon in complete genomicsTypical
- rs1792124SORL1 · 121,570,811G;Gcommon in complete genomicsTypical
- rs3781835SORL1 · 121,577,545G;Gcommon in complete genomicsTypical
- rs1699103SORL1 · 121,581,217T;TnormalTypical
- rs11218350SORL1 · 121,581,942A;AnormalTypical
- rs3781838SORL1 · 121,582,808T;Tcommon in complete genomicsTypical
- rs10892759SORL1 · 121,593,379A;Areduced risk for Alzheimers?Minor
- rs1792113SORL1 · 121,594,237A;AnormalTypical
- rs726601SORL1 · 121,610,698C;CnormalTypical
- rs1784931SORL1 · 121,612,229C;Creduced risk for Alzheimers?Minor
- rs2276077HSPA8 · 123,062,109C;CNo summary available.Typical
- rs735665GRAMD1B · 123,490,689G;Gcommon on affy axiom dataTypical
- rs2126709ZNF202 · 123,725,219C;Ccommon on affy axiom dataTypical
- rs10893081ZNF202 · 123,742,322C;C2x increased risk for severe atherosclerosis; 1.2x increased risk for ischemic heart diseaseTypical
- rs12280105TMEM225 · 123,881,121G;Gcommon genotypeTypical
- rs544368SIAE · 124,668,099C;Ccommon on affy axiom dataTypical
- rs12282107SIAE · 124,669,377T;Tcommon genotypeTypical
- rs3923890ROBO3 · 124,870,514A;Alower social interactionMinor
- rs521102CHEK1 · 125,644,678G;GnormalTypical
- rs4937076LOC338667 · 125,956,807G;Gcommon in clinvarTypical
- rs8177400TIRAP · 126,292,695A;ANo summary available.Important
- rs8177374TIRAP · 126,292,948T;Tresistance to several diseasesImportant
- rs620875MIR3167 · 126,989,261A;Acommon on affy axiom dataTypical
- rs7927044127,891,771G;Gcommon in complete genomicsTypical
- rs6590330LOC105369566 · 128,441,164G;Gcommon in complete genomicsTypical
- rs1128334ETS1 · 128,459,064C;Ccommon on affy axiom dataTypical
- rs665440FLI1 · 128,712,662T;TnormalTypical
- rs1231254KCNJ1 · 128,839,052T;Tcommon in clinvarTypical
- rs59172778KCNJ1 · 128,839,231A;GharmlessMinor
- rs6590357C11orf45 · 128,911,444C;Ccommon in complete genomicsTypical
- rs7118824KCNJ5 · 128,912,083G;Gcommon in complete genomicsTypical
- rs4937391KCNJ5 · 128,916,399G;Gcommon in clinvarTypical
- rs2298566SNX19 · 130,880,747A;Cincreased risk of coronary heart disease; better response to statinsWorth knowing
- rs11601906NTM · 131,455,352C;Ccommon genotypeTypical
- rs4397868133,697,090T;Tcommon on affy axiom dataTypical
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.