Chromosome 7
437 well-documented SNPs on chromosome 7, in order of position (GRCh38).
- rs3735684CYP2W1 · 985,219A;Gassociated with increased colorectal cancer riskMinor
- rs4866NUDT1 · 2,249,951G;GNo summary available.Typical
- rs645106SDK1 · 4,150,281C;Ccommon in complete genomicsTypical
- rs1059060PMS2 · 5,977,709T;Tcommon in complete genomicsTypical
- rs17420802PMS2 · 5,977,709T;Tcommon in clinvarTypical
- rs2228006PMS2 · 5,987,144T;Tcommon in clinvarTypical
- rs1805319PMS2 · 5,997,349G;Gcommon in clinvarTypical
- rs63750871PMS2 · 6,002,590C;TLynch syndromeVery important
- rs6953213LOC101927354 · 7,273,854G;Gcommon genotypeTypical
- rs17168526COL28A1 · 7,531,789T;Tcommon genotypeTypical
- rs37973GLCCI1 · 7,968,245A;Apossibly better response to inhaled corticosteroids in asthmaWorth knowing
- rs17143586ICA1 · 8,137,767C;Ccommon genotypeTypical
- rs10245124LOC105375144 · 8,602,724T;Tcommon genotypeTypical
- rs99185089,499,649C;Ccommon in complete genomicsTypical
- rs6971925DGKB · 14,406,292C;Ccommon in complete genomicsTypical
- rs7781293TMEM195 · 15,451,358A;Ccommon in complete genomicsTypical
- rs10486776LOC101927558 · 15,703,161G;Gcommon on affy axiom dataTypical
- rs17169056LOC105375167 · 15,751,201A;Acommon in complete genomicsTypical
- rs35681285ISPD · 16,287,021T;Tcommon genotypeTypical
- rs10270805SOSTDC1 · 16,460,517G;Gcommon in complete genomicsTypical
- rs16878759LOC105375168 · 16,463,459T;Tcommon in complete genomicsTypical
- rs4410790LOC101927609 · 17,244,953T;TNo summary available.Worth knowing
- rs6968865LOC101927609 · 17,247,645A;TAssociated with (slightly) increased coffee consumptionMinor
- rs2066853AHR · 17,339,486G;GNo summary available.Typical
- rs12155400HDAC9 · 18,389,298A;Acommon genotypeTypical
- rs213273HDAC9 · 18,464,885A;Acommon genotypeTypical
- rs2073963HDAC9 · 18,838,251G;Gincreased risk of baldnessWorth knowing
- rs2107595TWIST1 · 19,009,765A;ANo summary available.Typical
- rs430TWIST1 · 19,066,916G;GNo summary available.Typical
- rs38152LOC101927668 · 20,007,952A;Acommon on affy axiom dataTypical
- rs2108258ABCB5 · 20,752,375A;Acommon genotypeTypical
- rs13245023LINC01162 · 20,845,476C;Ccommon genotypeTypical
- rs17144465SP4 · 21,464,809A;ANo summary available.Typical
- rs6461593DNAH11 · 21,664,387T;TNo summary available.Typical
- rs368331DNAH11 · 21,703,356A;Acommon on affy axiom dataTypical
- rs1049955922,069,841G;Gcommon in complete genomicsTypical
- rs694914922,709,538G;Gcommon in complete genomicsTypical
- rs2069827IL6 · 22,725,837G;GNo summary available.Typical
- rs1800796LOC541472 · 22,726,627C;Cslightly increased risk for abdominal aortic aneurysm reportedMinor
- rs1800795IL6 · 22,727,026C;Cless IL6; certain risks, see detailsWorth knowing
- rs2069830IL6 · 22,727,518C;Ccommon in complete genomicsTypical
- rs1524107IL6 · 22,728,600C;Ccommon in complete genomicsTypical
- rs2066992IL6 · 22,728,630G;Gcommon in complete genomicsTypical
- rs13306435IL6 · 22,731,420T;Tcommon in complete genomicsTypical
- rs2069849IL6 · 22,731,537C;Ccommon genotypeTypical
- rs2069861IL6 · 22,732,035C;CNo summary available.Typical
- rs2286492FAM126A · 22,945,391A;Acommon in clinvarTypical
- rs886448LOC107986777 · 24,200,546G;Gcommon genotypeTypical
- rs16139NPY · 24,285,260T;Tcommon in clinvarTypical
- rs1468271NPY · 24,287,362T;TNo summary available.Typical
- rs754554DFNA5 · 24,719,199G;Gcommon in clinvarTypical
- rs1861525CYCS · 25,121,983A;Acommon in clinvarTypical
- rs101553726,143,201G;Gcommon in complete genomicsTypical
- rs11763963LOC101928077 · 26,605,814T;Tcommon in complete genomicsTypical
- rs10951154HOXA1 · 27,095,695C;Ccommon in clinvarTypical
- rs1322578327,290,437C;Ccommon in complete genomicsTypical
- rs1156402427,295,942T;TNo summary available.Typical
- rs1742847127,298,248G;Gcommon genotypeTypical
- rs2835722527,362,837T;Tcommon in complete genomicsTypical
- rs10486607CPVL · 29,144,873C;Ccommon on affy axiom dataTypical
- rs3750103CHN2 · 29,480,313A;Acommon genotypeTypical
- rs740145WIPF3 · 29,881,908G;Gcommon genotypeTypical
- rs2075822NOD1 · 30,451,144A;Acommon in complete genomicsTypical
- rs1049402GARS · 30,595,045C;Ccommon in clinvarTypical
- rs100059730,897,563T;Tcommon in complete genomicsTypical
- rs4988496GHRHR · 30,969,071G;Gcommon in complete genomicsTypical
- rs2267735ADCYAP1R1 · 31,095,890C;CAssociated with PTSD, hyperarousal, impaired fear discrimination in traumatized females, but not malesWorth knowing
- rs215738PDE1C · 32,404,823A;Acommon genotypeTypical
- rs17170316BBS9 · 33,633,653G;Gcommon in complete genomicsTypical
- rs136221235,265,695G;Gcommon on affy axiom dataTypical
- rs6948404AOAH · 36,570,887T;Tcommon on affy axiom dataTypical
- rs696357336,788,795G;GNo summary available.Typical
- rs1732966936,812,324A;ANo summary available.Typical
- rs13230047ELMO1 · 36,921,715C;Ccommon in complete genomicsTypical
- rs10488031ELMO1 · 37,037,249G;Gcommon in complete genomicsTypical
- rs4723619ELMO1 · 37,226,747T;Tcommon in complete genomicsTypical
- rs2392492ELMO1 · 37,325,592G;GNo summary available.Typical
- rs6974491ELMO1 · 37,334,906A;AHigher risk of coeliac and/or inflammatory bowel diseaseMinor
- rs11984075ELMO1 · 37,397,251A;ANo summary available.Typical
- rs6951258GPR141 · 37,717,954T;Tcommon genotypeTypical
- rs16879765EPDR1 · 37,949,493T;TSomewhat higher (~3x) risk for Dupuytren's DiseaseImportant
- rs11984145VPS41 · 38,795,435C;Ccommon on affy axiom dataTypical
- rs9986786POU6F2 · 39,197,987C;CNo summary available.Typical
- rs1048671541,439,010G;Gcommon in complete genomicsTypical
- rs472405541,582,932T;Tcommon genotypeTypical
- rs3735361GLI3 · 41,961,326C;Ccommon in clinvarTypical
- rs3823720GLI3 · 41,961,573G;Gcommon in clinvarTypical
- rs929387GLI3 · 41,966,080G;Gcommon in clinvarTypical
- rs10951671GLI3 · 42,190,347C;CNo summary available.Typical
- rs10232743URGCP-MRPS24 · 43,871,283C;Ccommon genotypeTypical
- rs10250779PGAM2 · 44,065,297A;Apossible exercise-inducing cramping in African-AmericansWorth knowing
- rs193922317GCK · 44,149,778C;Ccommon in clinvarTypical
- rs1799884GCK · 44,189,469T;T2.7x increased risk for Type 2 Diabetes. Mothers have babies 54g heavier.Important
- rs217434NPC1L1 · 44,513,639A;Acommon in clinvarTypical
- rs2072183NPC1L1 · 44,539,581G;Gcommon in clinvarTypical
- rs2107732CCM2 · 45,038,379G;Gcommon on affy axiom dataTypical
- rs4988515IGFBP1 · 45,893,001C;CNo summary available.Typical
- rs2854747IGFBP3 · 45,920,318G;G2326.08ng/mL of IGFBP-3 in plasmaMinor
- rs1722146LOC102723446 · 46,032,946A;Acommon in complete genomicsTypical
- rs6964415LOC107986792 · 46,202,985T;Tcommon on affy axiom dataTypical
- rs17513961LOC105375265 · 46,352,969T;TNo summary available.Typical
- rs11978267IKZF1 · 50,398,606G;Gpossible increased risk for infant acute myeloid leukemia (AML)Worth knowing
- rs4132601IKZF1 · 50,402,906G;Gmoderately (~2.5x) increased risk for acute lymphoblastic leukemiaWorth knowing
- rs11761683DDC · 50,475,181T;TMigraineMinor
- rs12718541DDC · 50,482,446A;ANicotine dependenceMinor
- rs6264DDC · 50,544,037C;Ccommon in complete genomicsTypical
- rs2044859DDC · 50,544,864A;AMigraineMinor
- rs11974297DDC · 50,550,562G;GMigraineMinor
- rs2329340DDC · 50,552,531T;TMMinor
- rs494808850,959,497A;ANo summary available.Typical
- rs40600151,938,719C;Ccommon genotypeTypical
- rs67983054,607,180C;Ccommon genotypeTypical
- rs225258654,911,231T;T1.4x higher risk for glioma developmentMinor
- rs763317EGFR · 55,027,504A;A3.5x increased lung cancer risk for never-smoking femalesTypical
- rs11979158EGFR · 55,091,656A;Acommon in complete genomicsTypical
- rs6958497EGFR · 55,094,053T;Tcommon in complete genomicsTypical
- rs3735061EGFR · 55,096,174G;Gcommon in complete genomicsTypical
- rs2072454EGFR · 55,146,655C;Ccommon in clinvarTypical
- rs2227983EGFR · 55,161,562G;Gcommon in clinvarTypical
- rs1050171EGFR · 55,181,370G;Gcommon in clinvarTypical
- rs17290699EGFR · 55,201,204A;Acommon in complete genomicsTypical
- rs2293347EGFR · 55,201,223C;Camong NSCLC patients, better Gefitinib response; commonMinor
- rs4947534PSPH · 56,011,401T;Tcommon in clinvarTypical
- rs6960379LOC105375323 · 64,290,139T;Tcommon in complete genomicsTypical
- rs9530GUSB · 65,960,907A;Acommon in clinvarTypical
- rs696161167,961,336T;Tcommon in complete genomicsTypical
- rs140315568,585,426G;Gcommon genotypeTypical
- rs2293507AUTS2 · 70,763,034G;Gcommon in complete genomicsTypical
- rs13238203TYW1B · 72,664,689C;Ccommon in complete genomicsTypical
- rs6943090FKBP6 · 73,332,645C;Ccommon genotypeTypical
- rs2240466BAZ1B · 73,441,939G;Gcommon on affy axiom dataTypical
- rs714052BAZ1B · 73,450,539A;Acommon on affy axiom dataTypical
- rs13233571BCL7B · 73,556,901C;Ccommon on affy axiom dataTypical
- rs17145738TBL2 · 73,568,544C;Ccommon on affy axiom dataTypical
- rs2071307ELN · 74,056,384G;Gcommon in clinvarTypical
- rs2856728ELN · 74,056,452C;Ccommon in clinvarTypical
- rs2522943CLIP2 · 74,400,419C;Ccommon in complete genomicsTypical
- rs236670POM121C · 75,430,050T;TNo summary available.Typical
- rs237238HIP1 · 75,582,098A;Acommon in complete genomicsTypical
- rs2302009CCL26 · 75,769,680C;C4.6x risk of eosinophilic esophagitisMinor
- rs1057868POR · 75,985,688T;T1.6x higher overall CYP3A activityMinor
- rs17685POR · 75,986,787G;Gcommon in clinvarTypical
- rs2868371HSPB1 · 76,301,442C;Ccommon in complete genomicsTypical
- rs9640663PTPN12 · 77,618,504A;GNo summary available.Typical
- rs2691543MAGI2 · 78,335,471T;Tcommon on affy axiom dataTypical
- rs17150687MAGI2 · 78,413,974A;Acommon in complete genomicsTypical
- rs11525066MAGI2 · 78,546,660G;Gcommon on affy axiom dataTypical
- rs1496766MAGI2 · 78,702,149T;Tcommon genotypeTypical
- rs1334512CD36 · 80,638,588G;G0.37x decreased risk for severe malariaTypical
- rs3173798CD36 · 80,656,534T;Tcommon in clinvarTypical
- rs11574703CD36 · 80,657,592T;Tcommon genotypeTypical
- rs3211892CD36 · 80,661,053A;Acommon in clinvarTypical
- rs3211908CD36 · 80,664,600C;CNo summary available.Typical
- rs3211938CD36 · 80,671,133T;Tcommon in complete genomicsTypical
- rs236685880,711,306A;Acommon genotypeTypical
- rs7779029SEMA3C · 80,902,796T;Tcommon in clinvarTypical
- rs12536657HGF · 81,720,892A;Ahypermetropia risk - longsightednessWorth knowing
- rs2286194HGF · 81,726,133T;Tcommon in complete genomicsTypical
- rs1750110881,774,578G;GNo summary available.Typical
- rs797821SEMA3A · 83,961,536T;Tcommon in clinvarTypical
- rs7804122SEMA3A · 84,005,397A;Acommon in complete genomicsTypical
- rs17159614SEMA3D · 85,096,186C;Ccommon in complete genomicsTypical
- rs2228595LOC107984122 · 86,786,671C;Ccommon in complete genomicsTypical
- rs11773103DMTF1 · 87,192,664A;Acommon in complete genomicsTypical
- rs31653ABCB4 · 87,403,297A;Acommon in clinvarTypical
- rs2109505ABCB4 · 87,450,090T;Tcommon in clinvarTypical
- rs1202283ABCB4 · 87,452,976G;Gcommon in clinvarTypical
- rs3842ABCB1 · 87,504,050T;TNo summary available.Typical
- rs28364274ABCB1 · 87,504,335C;Ccommon in complete genomicsTypical
- rs1045642ABCB1 · 87,509,329A;Aaltered drug metabolism and bioavailability; moderately increased risk for certain cancersImportant
- rs2229107ABCB1 · 87,509,343A;ANo summary available.Typical
- rs2235067ABCB1 · 87,520,606T;TNo summary available.Typical
- rs4148740ABCB1 · 87,522,787G;GNo summary available.Typical
- rs7787082ABCB1 · 87,527,735A;ANo summary available.Typical
- rs2032583ABCB1 · 87,531,245G;GNo summary available.Typical
- rs2032582ABCB1 · 87,531,302T;Trare genotype, on a triallelic snpMinor
- rs4148739ABCB1 · 87,531,733C;Tpossibly, inpatients more likely to remit on certain antidepressantsMinor
- rs11983225ABCB1 · 87,532,204C;CNo summary available.Typical
- rs10248420ABCB1 · 87,535,670A;Apossibly less likely to remit on certain antidepressantsMinor
- rs2235040ABCB1 · 87,536,434T;Tpossibly higher chances of remission only for inpatients on certain antidepressantsMinor
- rs12720067ABCB1 · 87,540,040T;TNo summary available.Typical
- rs1128503ABCB1 · 87,550,285G;GnormalTypical
- rs2229109ABCB1 · 87,550,493C;Ccommon in clinvarTypical
- rs2235015ABCB1 · 87,570,248C;Ccommon/normalTypical
- rs9282564ABCB1 · 87,600,124T;Tcommon on affy axiom dataTypical
- rs2214102ABCB1 · 87,600,185C;Ccommon in complete genomicsTypical
- rs3213619ABCB1 · 87,600,877A;Acommon in complete genomicsTypical
- rs10248351ZNF804B · 88,852,128T;Tcommon in complete genomicsTypical
- rs1406503ZNF804B · 88,931,564G;Gcommon on affy axiom dataTypical
- rs6959888ZNF804B · 88,967,071A;Acommon on affy axiom dataTypical
- rs6964587AKAP9 · 92,001,306G;Gcommon in clinvarTypical
- rs267607203KRIT1 · 92,222,870A;GCerebral Cavernous Malformation mutationVery important
- rs61750420PEX1 · 92,501,562T;Tperoxisomal biogenesis disorder (Zellweger) alleleVery important
- rs10CDK6 · 92,754,574C;CNo summary available.Typical
- rs180275GNGT1 · 93,906,158G;GNo summary available.Typical
- rs1801182COL1A2 · 94,398,387T;Tcommon in clinvarTypical
- rs42524COL1A2 · 94,413,927C;Ccommon in clinvarTypical
- rs2621215COL1A2 · 94,426,732T;Tcommon/normalTypical
- rs662PON1 · 95,308,134T;T~2x higher risk of of coronary heart disease reported in some studies, but lower risk seen in other studiesWorth knowing
- rs854560PON1 · 95,316,772A;Ahigher risk for heart disease, diabetic retinopathyWorth knowing
- rs705381PON1 · 95,324,637C;CnormalTypical
- rs13306702PON2 · 95,404,734C;Ccommon in complete genomicsTypical
- rs7493PON2 · 95,405,463G;Gcommon in clinvarTypical
- rs12026PON2 · 95,411,704G;Gcommon in clinvarTypical
- rs17876142PON2 · 95,411,704G;GNo summary available.Typical
- rs13231718DYNC1I1 · 95,971,056T;Tcommon genotypeTypical
- rs80338727SLC25A13 · 96,121,695T;TCitrullinemia type II/citrin deficiency; neonatal and/or adult-onsetVery important
- rs1759830696,952,499C;Ccommon on affy axiom dataTypical
- rs1048600397,600,466C;Ccommon in complete genomicsTypical
- rs13438327OCM2 · 97,991,379G;Gcommon in complete genomicsTypical
- rs7809799KPNA7 · 99,162,881A;Acommon on affy axiom dataTypical
- rs740160ARPC1A · 99,360,257C;Ccommon on affy axiom dataTypical
- rs7792939GS1-259H13.2 · 99,610,253T;Tcommon on affy axiom dataTypical
- rs28365085CYP3A5 · 99,648,351G;GCYP3A5*3F homozygote; nonexpressor for CYP3A5Worth knowing
- rs45593941CYP3A5 · 99,648,351G;GCYP3A5*3F homozygote; nonexpressor for CYP3A5Worth knowing
- rs28365083CYP3A5 · 99,652,613T;TCYP3A5*2 homozygote; nonexpressor for CYP3A5Worth knowing
- rs41303343CYP3A5 · 99,652,770A;AMiscall in 23andMe v4 data; otherwise, CYP3A5*7 homozygote; nonexpressor for CYP3A5Worth knowing
- rs10264272CYP3A5 · 99,665,212T;TCYP3A5*6 homozygote; nonexpressor for CYP3A5Worth knowing
- rs56411402CYP3A5 · 99,665,237C;CCYP3A5*4 homozygote; nonexpressor for CYP3A5Worth knowing
- rs776746CYP3A5 · 99,672,916C;CCYP3A5*3 homozygote; CYP3A5 non-expressorWorth knowing
- rs28383468CYP3A5 · 99,676,192A;ACYP3A5*H30Y homozygote; nonexpressor for CYP3A5Worth knowing
- rs2257401CYP3A7 · 99,709,062G;Gcommon in complete genomicsTypical
- rs45446698ZSCAN25 · 99,735,325G;GCarrier of two CYP3A7*1C alleles; possibly reduced contraceptive effectiveness and moderately increased cancer riskImportant
- rs67666821CYP3A4 · 99,758,183T;TCYP3A4*20 homozygote; side effects likely from many drugsVery important
- rs4986913CYP3A4 · 99,760,836G;GnormalTypical
- rs4986910CYP3A4 · 99,760,901G;GCYP3A4*3 homozygoteTypical
- rs1041988CYP3A4 · 99,760,943G;GCYP3A4*_23139T>C(I431T) homozygoteTypical
- rs4986909CYP3A4 · 99,762,047G;GnormalTypical
- rs12721629CYP3A4 · 99,762,177A;ACYP3A4*12 homozygoteWorth knowing
- rs45614732CYP3A4 · 99,762,177G;GNo summary available.Typical
- rs4646440CYP3A4 · 99,763,247G;Gcommon in complete genomicsTypical
- rs2242480CYP3A4 · 99,763,843C;CnormalTypical
- rs28371759CYP3A4 · 99,764,003G;GCYP3A4*18 homozygoteTypical
- rs3208363CYP3A4 · 99,767,175C;CCYP3A4*_16907T>G(S252A) homozygoteTypical
- rs4646437CYP3A4 · 99,767,460G;Gcommon in complete genomicsTypical
- rs3208361CYP3A4 · 99,768,447T;TnormalTypical
- rs4987161CYP3A4 · 99,768,458G;GCYP3A4*17 homozygoteTypical
- rs4986908CYP3A4 · 99,769,769T;TCYP3A4*_14313G>A(E174H) homozygoteTypical
- rs4986907CYP3A4 · 99,769,804T;TCYP3A4*15A homozygoteTypical
- rs3091339CYP3A4 · 99,772,622T;TnormalTypical
- rs2740574CYP3A · 99,784,473C;C2.5x increased risk for prostate or ovarian cancer; CYP3A4*1B homozygoteWorth knowing
- rs680055CYP3A43 · 99,859,982C;CNo summary available.Typical
- rs17342647CYP3A43 · 99,861,633C;Ccommon in complete genomicsTypical
- rs17277546TRIM4 · 99,891,948G;Gcommon in complete genomicsTypical
- rs1637001STAG3 · 100,210,528A;Acommon in complete genomicsTypical
- rs13222543ZCWPW1 · 100,417,834C;Ccommon genotypeTypical
- rs2075674TFR2 · 100,627,408G;Gcommon in clinvarTypical
- rs80338885TFR2 · 100,628,294C;TLikely miscall in DNA chip data; see text of main rs-pageMinor
- rs314370SLC12A9 · 100,855,586T;Tcommon on affy axiom dataTypical
- rs12666989UFSP1 · 100,889,133G;Gcommon on affy axiom dataTypical
- rs1799805ACHE · 100,893,176G;Gcommon in clinvarTypical
- rs1799889SERPINE1 · 101,126,430-;-MI riskTypical
- rs6092SERPINE1 · 101,128,436G;Gcommon on affy axiom dataTypical
- rs6090SERPINE1 · 101,128,442G;Gcommon in clinvarTypical
- rs2227667SERPINE1 · 101,131,468G;GNo summary available.Typical
- rs2227692SERPINE1 · 101,135,963C;T1.6x higher risk for diffuse gastric cancerMinor
- rs11178SERPINE1 · 101,137,803T;Tcommon in clinvarTypical
- rs7242SERPINE1 · 101,138,164T;Tcommon in clinvarTypical
- rs17135437COL26A1 · 101,472,713C;Ccommon genotypeTypical
- rs736707RELN · 103,489,956A;Acommon in complete genomicsTypical
- rs2229860RELN · 103,565,380G;Gcommon in complete genomicsTypical
- rs362691RELN · 103,610,714G;Gcommon in complete genomicsTypical
- rs7341475RELN · 103,764,368G;G1.58x increased schizophrenia risk for womenMinor
- rs3914132RELN · 103,886,922C;CLower otosclerosis riskWorth knowing
- rs4298437RELN · 103,985,430C;CNo summary available.Typical
- rs10953454LHFPL3 · 104,863,366G;Gcommon in complete genomicsTypical
- rs11983798ATXN7L1 · 105,640,741G;Gcommon genotypeTypical
- rs10270308CDHR3 · 106,030,821T;Tcommon genotypeTypical
- rs10487818NAMPT · 106,269,615A;Acommon in complete genomicsTypical
- rs17153527106,855,364T;Tcommon on affy axiom dataTypical
- rs7798500107,021,638A;Acommon in complete genomicsTypical
- rs13224682PRKAR2B · 107,122,773A;Acommon on affy axiom dataTypical
- rs3815148COG5 · 107,297,975C;C1.34x increased risk of OsteoarthritisImportant
- rs4730250DUS4L · 107,567,250A;Acommon on affy axiom dataTypical
- rs10953541BCAP29 · 107,604,100C;Ccommon on affy axiom dataTypical
- rs60284988SLC26A4-AS1 · 107,660,756T;Tcommon in clinvarTypical
- rs111033308SLC26A4 · 107,695,984G;Gcommon in clinvarTypical
- rs12539530NRCAM · 108,336,117G;Gcommon in complete genomicsTypical
- rs2216259NRCAM · 108,375,106A;Acommon in complete genomicsTypical
- rs1859767NRCAM · 108,447,879A;Acommon in complete genomicsTypical
- rs1404697108,904,404G;Gcommon in complete genomicsTypical
- rs848353108,908,603A;Acommon in complete genomicsTypical
- rs17157913IMMP2L · 110,700,918T;Tcommon genotypeTypical
- rs12531640IMMP2L · 110,839,479G;Gcommon on affy axiom dataTypical
- rs10428959DOCK4 · 112,037,851C;Ccommon genotypeTypical
- rs3128396IFRD1 · 112,430,182G;Gcommon in complete genomicsTypical
- rs17159640IFRD1 · 112,446,278A;Acommon on affy axiom dataTypical
- rs5009270112,519,123A;Apossible risk of osteoarthritis of the hip.Minor
- rs1799999PPP1R3A · 113,878,379A;Ainsulin resistanceImportant
- rs2974938PPP1R3A · 113,878,447T;Tcommon in complete genomicsTypical
- rs2974944PPP1R3A · 113,879,664T;Tcommon in complete genomicsTypical
- rs2974942PPP1R3A · 113,879,741T;Tcommon in complete genomicsTypical
- rs10227893FOXP2 · 114,630,022T;Tcommon in complete genomicsTypical
- rs3807987CAV1 · 116,539,780G;Gcommon in complete genomicsTypical
- rs4730751CAV1 · 116,540,796A;AFor kidney donors, 2x more likely to result in allograft rejectionWorth knowing
- rs1858830MET · 116,672,385C;C2x risk of autism reported by some (but not other) publicationsWorth knowing
- rs2237717MET · 116,765,333T;Treduced abilities related to neurocognition and ability to recognize facesImportant
- rs1621MET · 116,797,552G;Gcommon in clinvarTypical
- rs6566MET · 116,798,364G;Gcommon in clinvarTypical
- rs7782376116,937,070G;Gcommon in complete genomicsTypical
- i4000305CFTR · 117,227,860A;Aa treatable form of cystic fibrosisVery important
- i4000320CFTR · 117,242,922A;ACystic FibrosisVery important
- rs2228946WNT2 · 117,278,031C;Ccommon in complete genomicsTypical
- rs193922501CFTR · 117,480,108C;Tcystic fibrosis carrier (most likely)Important
- rs143456784CFTR · 117,504,324C;Tcystic fibrosis carrier (most likely)Important
- rs121908798CFTR · 117,530,950G;TATcarrier of a cystic fibrosis alleleImportant
- rs78655421CFTR · 117,530,975A;GPossible cystic fibrosis allele carrier, but of low penetranceImportant
- rs35516286CFTR · 117,531,068T;Tcommon in clinvarTypical
- rs75053309CFTR · 117,540,309A;Ccystic fibrosis carrierImportant
- rs74551128CFTR · 117,548,795A;ACystic fibrosisVery important
- rs213950CFTR · 117,559,479A;Avery slight (1.1x) increase in type-1 diabetes riskTypical
- rs199826652CFTR · 117,559,591-;-Cystic Fibrosis; homozygote for delta F-508 mutationVery important
- rs113993960CFTR · 117,559,592-;-Cystic Fibrosis; homozygote for delta F-508 mutationVery important
- rs332CFTR · 117,559,593TCT;TCTHomozygous for F508C variant of cystic fibrosis gene; benignTypical
- rs10487372CFTR · 117,560,845C;Ccommon in complete genomicsTypical
- rs10281281CFTR · 117,564,408A;Acommon in complete genomicsTypical
- rs75527207CFTR · 117,587,806A;ADouble homozygote for cystic fibrosis G551D alleleVery important
- rs193922504CFTR · 117,587,827C;Tcystic fibrosis carrier (most likely)Important
- rs145449046CFTR · 117,592,541C;Gcystic fibrosis carrier (most likely)Important
- rs1042077CFTR · 117,595,001T;Tcommon/normalTypical
- rs193922506CFTR · 117,595,036A;Gcystic fibrosis carrier (most likely)Important
- rs144055758CFTR · 117,610,625A;Gcystic fibrosis carrier (most likely)Important
- rs78802634CFTR · 117,611,707A;Gcystic fibrosis carrierImportant
- rs121908789CFTR · 117,642,493-;Tcarrier of a cystic fibrosis alleleImportant
- rs11971167CFTR · 117,642,528A;Gcarrier of cystic fibrosis alleleImportant
- rs77010898CFTR · 117,642,566A;GCystic fibrosis allele (carrier)Important
- rs10155917CFTR · 117,642,710T;Tcommon in complete genomicsTypical
- rs10244810CFTR · 117,645,297A;Acommon in complete genomicsTypical
- rs10234329CFTR · 117,668,151A;Acommon in complete genomicsTypical
- rs17142462119,966,578C;Ccommon genotypeTypical
- rs2908004WNT16 · 121,329,715G;Gweaker bonesWorth knowing
- rs2707466WNT16 · 121,339,035T;Tstronger bonesWorth knowing
- rs7776725FAM3C · 121,393,067C;Cweaker bonesWorth knowing
- rs846664TAS2R16 · 122,995,119A;Acommon in clinvarTypical
- rs17147033124,366,686C;Ccommon in complete genomicsTypical
- rs17691394GRM8 · 126,684,537A;Acommon in complete genomicsTypical
- rs17864092GRM8 · 126,999,550T;Tcommon in complete genomicsTypical
- rs1592377GRM8 · 127,251,397A;ANo summary available.Typical
- rs2233580PAX4 · 127,613,496C;TReported to slightly increase (1.5x) risk for T2D in AsiansMinor
- rs2233578PAX4 · 127,614,497G;Gcommon in complete genomicsTypical
- rs2167270LEP · 128,241,296A;A0.79x reduced risk for colon cancerTypical
- rs10244329LEP · 128,248,636A;Tcommon in complete genomicsTypical
- rs17151919LEP · 128,254,539G;Gcommon in complete genomicsTypical
- rs10954174LEP · 128,256,483A;Acommon in clinvarTypical
- rs2228075IMPDH1 · 128,394,575C;Ccommon in clinvarTypical
- rs6971091FAM71F1 · 128,723,233A;A>2x increased risk for familial obesityTypical
- rs339097CALU · 128,759,170A;Acommon in complete genomicsTypical
- rs2291569FLNC · 128,848,680G;Gcommon on affy axiom dataTypical
- rs729302128,928,906A;C0.89x decreased risk of developing rheumatoid arthritisMinor
- rs6953165IRF5 · 128,938,156C;Ccommon in complete genomicsTypical
- rs2004640IRF5 · 128,938,247T;T1.4x increased risk for SLEWorth knowing
- rs41298401IRF5 · 128,938,253C;Ccommon in complete genomicsTypical
- rs10488631TNPO3 · 128,954,129C;C2x increased risk of developing SLE; 3.2x increased risk of developing primary biliary cirrhosis; and 3.4x increased risk of developing Sjögren's syndromeImportant
- rs2280714TNPO3 · 128,954,671T;T1.4x increased risk of SLEMinor
- rs12531711TNPO3 · 128,977,412A;Acommon in complete genomicsTypical
- rs13246321129,061,277T;Tcommon in complete genomicsTypical
- rs12537284129,077,852G;Gcommon in complete genomicsTypical
- rs17710891SMO · 129,209,348G;Gcommon in clinvarTypical
- rs11766298AHCYL2 · 129,365,006C;Ccommon genotypeTypical
- rs2171492CPA4 · 130,310,900T;THigher prostate cancer riskWorth knowing
- rs7807274MKLN1 · 131,336,340G;Gcommon genotypeTypical
- rs3847109MKLN1 · 131,418,715G;Gcommon in complete genomicsTypical
- rs11761231131,685,280A;ANo summary available.Typical
- rs17166082132,028,601G;Gcommon genotypeTypical
- rs7341474PLXNA4 · 132,171,454C;Ccommon in complete genomicsTypical
- rs958408EXOC4 · 133,456,164G;Gcommon in complete genomicsTypical
- rs11770757EXOC4 · 134,063,193G;GNo summary available.Typical
- rs17231212C7orf49 · 135,100,989T;TNo summary available.Typical
- rs324640CHRM2 · 137,004,249A;ANo summary available.Typical
- rs324650CHRM2 · 137,008,914A;TNo summary available.Typical
- rs12673281LOC349160 · 137,074,042G;Gcommon in complete genomicsTypical
- rs161339137,370,779A;Acommon in complete genomicsTypical
- rs6467710DGKI · 137,519,073G;Gcommon in complete genomicsTypical
- rs834062DGKI · 137,542,904T;Tcommon in complete genomicsTypical
- rs357394138,364,642G;Gcommon on affy axiom dataTypical
- rs3807153ATP6V0A4 · 138,733,046A;Gcarrier of a benign changeMinor
- rs10258719ATP6V0A4 · 138,771,243A;Acommon in clinvarTypical
- rs13225917TTC26 · 139,166,872A;ARelatively rare genotype, please email info@snpedia.comImportant
- rs17837497TBXAS1 · 140,002,794G;Gcommon genotypeTypical
- rs121913355BRAF · 140,781,602C;TRasopathy; Cardio-facio-cutaneous syndromeVery important
- rs10246939TAS2R38 · 141,972,804T;Tpossibly unable to taste bitternessMinor
- rs1726866TAS2R38 · 141,972,905A;Apossible unable to taste bitterMinor
- rs713598TAS2R38 · 141,973,545G;GCan taste bitter.Minor
- rs2854536142,357,119A;APotential environmental trigger for autoimmune diseasesMinor
- rs111033566PRSS1 · 142,750,600A;CProblematic; maybe pathogenic for hereditary pancreatitis, maybe notWorth knowing
- rs144422014PRSS1 · 142,750,675A;GProbably benign, but possibly associated with hereditary pancreatitisWorth knowing
- rs111033565PRSS1 · 142,751,938A;GHereditary pancreatitisVery important
- rs8176038KEL · 142,943,026G;GKell blood group; Jsa/Jsa (aka Js(a+b-)) antigenMinor
- rs8176059KEL · 142,954,267G;Gcommon in clinvarTypical
- rs8176058KEL · 142,957,921A;AKELL blood group; K antigen (K/K)Worth knowing
- rs10282312CLCN1 · 143,320,714T;Tcommon on affy axiom dataTypical
- rs802568CNTNAP2 · 146,262,151T;Tcommon in complete genomicsTypical
- rs7799181CNTNAP2 · 146,351,738A;Acommon in complete genomicsTypical
- rs1718101CNTNAP2 · 146,425,696C;CNo summary available.Typical
- rs1358075CNTNAP2 · 146,438,846T;Tcommon genotypeTypical
- rs7794745CNTNAP2 · 146,792,514A;Tslightly increased risk for autismWorth knowing
- rs851715CNTNAP2 · 147,829,814T;Trisk of nonsense-word repetition problems if speech-impairedMinor
- rs10246256CNTNAP2 · 147,857,715C;CNo summary available.Typical
- rs2710102CNTNAP2 · 147,877,298A;ADelayed childhood speech.Worth knowing
- rs759178CNTNAP2 · 147,878,020C;Chigher risk of speech development delay and/or impairmentTypical
- rs17236239CNTNAP2 · 147,885,213G;Ghigher risk for speech development delay and/or impairmentWorth knowing
- rs2538976CNTNAP2 · 147,888,727T;TNo summary available.Typical
- rs2710117CNTNAP2 · 147,904,680A;Ahigher risk of speech development delay and/or impairmentTypical
- rs7807268148,560,956C;C1.4x risk for Crohn's diseaseWorth knowing
- rs855913149,506,571A;Areduced survival with ALSWorth knowing
- rs17173608RARRES2 · 150,339,575G;Glower visceral adipose tissueTypical
- rs2052129AOC1 · 150,851,884T;Trelated to Histamine intoleranceImportant
- rs10156191AOC1 · 150,856,517T;TAssociated with Response to Non-Steroidal Anti-Inflammatory Drugs, see text of rs-page for discussion. Indicates poor histamine breakdown due to decreased DAO activity, compared to the CC allele.Worth knowing
- rs1049742AOC1 · 150,857,465C;Ccommon on affy axiom dataTypical
- rs2968864150,925,074T;Tcommon on affy axiom dataTypical
- rs2968863150,926,049T;TPossibly slightly higher (2.4x) risk for atrial fibrillationWorth knowing
- rs1805123KCNH2 · 150,948,446T;Tcommon in clinvarTypical
- rs12720441KCNH2 · 150,950,216A;GRomano-Ward Long QT SyndromeVery important
- rs1137617KCNH2 · 150,951,110A;Tpotential cardiac arrhythmiaVery important
- rs9333649KCNH2 · 150,951,679C;TRomano-Ward Long QT SyndromeVery important
- rs731506LOC107986861 · 150,974,896A;Acommon in clinvarTypical
- rs4496877NOS3 · 150,983,418T;TFor type-1 diabetics, 1.6x increased nephropathy riskMinor
- rs2070744NOS3 · 150,992,991T;Tcardiovascular differencesWorth knowing
- rs3918226NOS3 · 150,993,088C;CNo summary available.Typical
- rs1799983NOS3 · 150,999,023G;Gnormal riskTypical
- rs3918227NOS3 · 151,003,858C;CNo summary available.Typical
- rs891512NOS3 · 151,011,001A;AHigher blood pressure than G;GImportant
- rs7830NOS3 · 151,012,483G;Gcommon in clinvarTypical
- rs2069454CDK5 · 151,055,895C;Ccommon in complete genomicsTypical
- rs3218536XRCC2 · 152,648,922T;Tlower risk for breast, ovarian cancerWorth knowing
- rs3218499XRCC2 · 152,655,054C;Ccommon in complete genomicsTypical
- rs3218408XRCC2 · 152,670,531A;Acommon in complete genomicsTypical
- rs6464375DPP6 · 153,928,758C;Ccommon in complete genomicsTypical
- rs6977820DPP6 · 154,374,935T;Tcommon in clinvarTypical
- rs10239794DPP6 · 154,508,809C;CProbably benign; one 2008 study reports 1.3x higher risk for ALSMinor
- rs10260404DPP6 · 154,513,713C;C1.60x risk of developing ALSWorth knowing
- rs6460013EN2 · 155,459,499G;GNo summary available.Typical
- rs1861973EN2 · 155,461,450C;CNo summary available.Typical
- rs9333613SHH · 155,807,597T;Tcommon in complete genomicsTypical
- rs10267337155,976,055C;Ccommon genotypeTypical
- rs10226930156,044,601T;Tcommon genotypeTypical
- rs1130495PTPRN2 · 158,167,219G;Gcommon 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.