Chromosome 5
386 well-documented SNPs on chromosome 5, in order of position (GRCh38).
- rs924607LOC100996325 · 609,978T;Tin childhood acute lymphoblastic leukemia patients, worse response to vincristineMinor
- rs2736100TERT · 1,286,401A;Ahigher risk of Interstitial lung disease, and testicular cancer, 2.1x risk of pulmonary fibrosisWorth knowing
- rs2853676TERT · 1,288,432C;CNo summary available.Typical
- rs2736098TERT · 1,293,971T;Tslightly increased risk for several types of cancersTypical
- rs402710CLPTM1L · 1,320,607C;CCommon, but higher lung cancer risk ?Minor
- rs401681CLPTM1L · 1,321,972C;C~1.2x increased risk for several types of cancerMinor
- rs31489CLPTM1L · 1,342,599A;C1.75-fold reduced risk of developing lung cancerWorth knowing
- rs27072SLC6A3 · 1,394,407C;C2x risk of severe alcohol withdrawal. Possible increased odds of ADHD.Worth knowing
- rs6869645SLC6A3 · 1,404,433C;Ccommon in complete genomicsTypical
- rs6347SLC6A3 · 1,411,297T;Tcommon in clinvarTypical
- rs27048SLC6A3 · 1,412,530C;C2x risk of severe alcohol withdrawalTypical
- rs37022SLC6A3 · 1,415,514A;Acommon in complete genomicsTypical
- rs464049SLC6A3 · 1,423,790G;Gdecreased risk of schizophrenia in limited studyMinor
- rs460000SLC6A3 · 1,432,710G;GBetter response to amphetamineWorth knowing
- rs403636SLC6A3 · 1,438,239C;Ccommon in complete genomicsTypical
- rs6350SLC6A3 · 1,443,084G;GNo summary available.Typical
- rs176825473,395,801T;TNo summary available.Typical
- rs17683231LOC285577 · 3,416,258T;TNo summary available.Typical
- rs17632091LINC01019 · 3,417,463G;GNo summary available.Typical
- rs65552594,198,004G;Gcommon genotypeTypical
- rs65552614,198,323C;Ccommon genotypeTypical
- rs2086310ADAMTS16 · 5,146,222G;Gcommon in complete genomicsTypical
- rs2964433ADAMTS16 · 5,237,484G;GNo summary available.Typical
- rs12518614FLJ33360 · 6,324,180A;ANo summary available.Typical
- rs16910536,677,052C;TIncreased risk of developing prostate cancerWorth knowing
- rs12520016LOC102724943 · 6,767,199G;GG allele associated with intermediate eye color and decreased risk of melanomaTypical
- rs111341786,834,054T;Tcommon in complete genomicsTypical
- rs13172324LOC105374645 · 7,368,732C;Ccommon genotypeTypical
- rs13166360ADCY2 · 7,520,768G;GHomozygous wild type at the ADCY2 geneTypical
- rs326155ADCY2 · 7,816,532A;ANo summary available.Typical
- rs1801394MTRR · 7,870,860G;G1.4x higher risk for meningiomasWorth knowing
- rs1532268MTRR · 7,878,066T;Tincreased riskWorth knowing
- rs2303080MTRR · 7,878,311T;Tcommon in clinvarTypical
- rs3776463MTRR · 7,885,114A;Acommon genotypeTypical
- rs162036MTRR · 7,885,846A;Acommon in complete genomicsTypical
- rs2287780MTRR · 7,889,191C;Ccommon in clinvarTypical
- rs10380MTRR · 7,897,078C;Ccommon in complete genomicsTypical
- rs1802059MTRR · 7,897,206G;Gcommon in clinvarTypical
- rs9332MTRR · 7,900,599G;Gcommon in complete genomicsTypical
- rs10520873MTRR · 7,901,117T;Tcommon in clinvarTypical
- rs26581618,133,581T;TNo summary available.Typical
- rs6896702SEMA5A · 9,331,736T;TIncreased risk of developing Parkinson's DiseaseWorth knowing
- rs105130259,623,510C;C>0.55x reduced risk for autismWorth knowing
- rs105130269,623,994C;Ccommon in complete genomicsTypical
- rs2607292MARCH6 · 10,372,506C;Ccommon in complete genomicsTypical
- rs1717697310,811,362C;Ccommon genotypeTypical
- rs4463179LOC105374660 · 13,505,322G;Gcommon in complete genomicsTypical
- rs3734110DNAH5 · 13,701,427T;Tcommon in clinvarTypical
- rs30168DNAH5 · 13,718,980G;Gcommon in clinvarTypical
- rs1530498DNAH5 · 13,902,111T;Tcommon in clinvarTypical
- rs339445DNAH5 · 13,944,403A;Acommon in clinvarTypical
- rs3045OTULIN · 14,711,166T;Tcommon in clinvarTypical
- rs74597815,285,305T;Tcommon genotypeTypical
- rs17651119MYO10 · 16,812,529C;Ccommon genotypeTypical
- rs17614462MYO10 · 16,913,746G;GNo summary available.Typical
- rs12109285CDH12 · 21,749,239T;Tcommon in complete genomicsTypical
- rs4701252CDH12 · 21,779,045T;Tcommon on affy axiom dataTypical
- rs291427623,542,602T;Tcommon genotypeTypical
- rs430705925,967,594T;T1.42x risk of AutismImportant
- rs96908826,389,153G;Gcommon genotypeTypical
- rs447980626,723,674C;Ccommon in complete genomicsTypical
- rs4867568LOC105374701 · 28,549,074C;Tdecreased risk of knee osteoporosisMinor
- rs2291109DROSHA · 31,532,322T;Tcommon in complete genomicsTypical
- rs700923NPR3 · 32,734,762A;Acommon in complete genomicsTypical
- rs16890196NPR3 · 32,739,555A;Acommon in complete genomicsTypical
- rs16891982SLC45A2 · 33,951,588C;Gif European, 7x more likely to have black hairWorth knowing
- rs17855902SLC45A2 · 33,951,588C;CNo summary available.Typical
- rs35390SLC45A2 · 33,955,221A;Acommon in complete genomicsTypical
- rs35391SLC45A2 · 33,955,568C;Ccommon in complete genomicsTypical
- rs28777SLC45A2 · 33,958,854A;Acommon in complete genomicsTypical
- rs26722SLC45A2 · 33,963,765C;Tperhaps darker eye, hair, skinWorth knowing
- rs2278008C1QTNF3-AMACR · 33,989,413C;Ccommon in clinvarTypical
- rs34677AMACR · 33,998,663G;GNo summary available.Typical
- rs2287939C1QTNF3-AMACR · 33,998,778G;GNo summary available.Typical
- rs10941112C1QTNF3-AMACR · 34,004,602C;Ccommon in clinvarTypical
- rs3195676C1QTNF3-AMACR · 34,007,995C;Ccommon in clinvarTypical
- rs37369AGXT2 · 35,037,010C;Ccommon in clinvarTypical
- rs1494558LOC105374724 · 35,860,966T;Tcommon in clinvarTypical
- rs193922641IL7R · 35,867,437G;Gcommon in clinvarTypical
- rs1494555IL7R · 35,871,088G;Gcommon in clinvarTypical
- rs6897932IL7R · 35,874,473T;T0.70x decreased risk for multiple sclerosisWorth knowing
- rs3194051IL7R · 35,876,172A;A>1.1x risk of type-1 diabetesMinor
- rs10491434IL7R · 35,877,812A;Acommon in clinvarTypical
- rs267759LMBRD2 · 36,137,518G;Gcommon in complete genomicsTypical
- rs36119840GDNF · 37,816,010G;Gcommon in complete genomicsTypical
- rs7715172EGFLAM · 38,452,792C;Ccommon genotypeTypical
- rs3729740LIFR · 38,496,535C;Ccommon in complete genomicsTypical
- rs2292016OSMR · 38,845,758G;Gcommon in complete genomicsTypical
- rs2278329OSMR · 38,921,686G;Gcommon in complete genomicsTypical
- rs2255280DAB2 · 39,394,887A;Acommon in complete genomicsTypical
- rs1005350239,979,070C;Ccommon genotypeTypical
- rs1992662PTGER4 · 40,393,750G;Gincreased risk for Crohn's diseaseTypical
- rs1723465740,401,407A;ANo summary available.Typical
- rs1992660PTGER4 · 40,414,965T;Tincreased risk for Crohn's diseaseTypical
- rs13188386GHR · 42,473,453G;GNo summary available.Typical
- rs4590183GHR · 42,626,104C;Cd3/d3GHR homozygote; possibly longer longevity, at least in malesWorth knowing
- rs6873545GHR · 42,631,162C;Cd3/d3GHR homozygote; possibly longer longevity, at least in malesWorth knowing
- rs6413484GHR · 42,699,868G;Gcommon in clinvarTypical
- rs6180GHR · 42,719,137A;Acommon in clinvarTypical
- rs441508444,662,413C;CNo summary available.Typical
- rs1094169445,197,677G;Gcommon on affy axiom dataTypical
- rs1783585351,877,490G;Gcommon genotypeTypical
- rs830884LOC105378964 · 52,724,562T;Tcommon genotypeTypical
- rs1551943ITGA1 · 52,899,203G;Gcommon in complete genomicsTypical
- rs1126643ITGA2 · 53,051,539C;Ccommon in clinvarTypical
- rs1801106ITGA2 · 53,062,927G;Gcommon in clinvarTypical
- rs788517ARL15 · 53,951,556C;Ccommon in complete genomicsTypical
- rs1694089ARL15 · 53,951,564A;Acommon in complete genomicsTypical
- rs2548621SNX18 · 54,606,509A;Acommon genotypeTypical
- rs88931256,736,057A;CVery slightly higher risk for breast cancerMinor
- rs2229882MAP3K1 · 56,872,885C;Ccommon genotypeTypical
- rs772635456,960,656C;Ccommon genotypeTypical
- rs6892553LOC102724122 · 57,514,311T;Tcommon genotypeTypical
- rs966221PDE4D · 60,206,693G;G1.5x increased stroke risk certain populationsMinor
- rs12188950PDE4D · 60,487,490C;Ccommon in complete genomicsTypical
- rs772953965,121,851T;Tcommon genotypeTypical
- rs13183791ADAMTS6 · 65,238,814C;CNo summary available.Typical
- rs1697144CD180 · 67,184,176C;Ccommon in complete genomicsTypical
- rs771757267,537,429G;Gcommon in complete genomicsTypical
- rs3730089PIK3R1 · 68,292,320G;Gcommon in clinvarTypical
- rs4916SMN2 · 70,076,526C;Ccommon in complete genomicsTypical
- rs7714670ARHGEF28 · 73,776,529T;Tcommon in clinvarTypical
- rs16871023ARHGEF28 · 73,919,412G;Gcommon in complete genomicsTypical
- rs820878HEXB · 74,685,445C;Ccommon in complete genomicsTypical
- rs11556045HEXB · 74,689,390A;Acommon in clinvarTypical
- rs3761740HMGCR · 75,336,308C;Ccommon in complete genomicsTypical
- rs17244841HMGCR · 75,347,030A;Amore responsive to statin treatmentTypical
- rs5908HMGCR · 75,356,374A;Acommon in complete genomicsTypical
- rs17238540HMGCR · 75,359,673G;Gless responsive to statin treatmentTypical
- rs2227831F2R · 76,727,669A;Acommon genotypeTypical
- rs1756862876,751,114T;Tcommon genotypeTypical
- rs4704397PDE8B · 77,222,617A;A0.26 muIU/ml higher TSHTypical
- rs1265591777,996,116G;Gcommon in complete genomicsTypical
- rs6453373AP3B1 · 78,129,204A;Acommon in clinvarTypical
- rs1065757ARSB · 78,885,654C;Ccommon in clinvarTypical
- rs2052550ARSB · 78,977,119C;Ccommon in complete genomicsTypical
- rs532964DMGDH · 79,044,463C;TNo summary available.Typical
- rs16876512BHMT · 79,111,438C;Ccommon in complete genomicsTypical
- rs6875201BHMT · 79,114,741A;Acommon in complete genomicsTypical
- rs470455979,517,086A;Acommon in complete genomicsTypical
- rs13358260LOC105379047 · 79,549,888T;Tcommon on affy axiom dataTypical
- rs1643649DHFR · 80,643,630T;Tcommon/normalTypical
- rs70991108DHFR · 80,654,344-;-high folic acid intake leads to high unmetabolized folic acid circulating levels, whereas low intake leads to low RBC folateMinor
- rs1650697DHFR · 80,654,962A;Acommon in clinvarTypical
- rs103275782,643,499G;Gcommon in complete genomicsTypical
- rs6869366TMEM167A · 83,075,927G;G>2x increased risk for bladder cancerTypical
- rs2075686TMEM167A · 83,076,927C;Ccommon in complete genomicsTypical
- rs9293329XRCC4 · 83,100,768G;GNo summary available.Typical
- rs3734091XRCC4 · 83,204,915G;Gcommon in complete genomicsTypical
- rs13178127XRCC4 · 83,293,613A;Acommon in complete genomicsTypical
- rs1728442083,417,201G;GNo summary available.Typical
- rs251124VCAN · 83,509,605T;TNo summary available.Typical
- rs173686VCAN · 83,515,681C;TNo summary available.Typical
- rs771752784,561,093A;Acommon on affy axiom dataTypical
- rs254467787,103,445G;GnormalTypical
- rs17421627LOC645323 · 88,551,768T;Tcommon on affy axiom dataTypical
- rs11951031MEF2C · 88,842,914C;Ccommon genotypeTypical
- rs1967256ADGRV1 · 91,003,406G;Gcommon in complete genomicsTypical
- rs1005554492,222,904G;GNo summary available.Typical
- rs1027643LOC105379082 · 92,558,085C;Ccommon in complete genomicsTypical
- rs486941993,231,833A;Acommon in complete genomicsTypical
- rs17376456KIAA0825 · 94,221,997A;Acommon in complete genomicsTypical
- rs6869388KIAA0825 · 94,474,503T;Tcommon in complete genomicsTypical
- rs147295ELL2 · 95,883,557C;Ccommon in complete genomicsTypical
- rs6235LOC101929710 · 96,393,194C;Ccommon in clinvarTypical
- rs6234PCSK1 · 96,393,270G;Gcommon in clinvarTypical
- rs6232PCSK1 · 96,416,081C;CHigher risk of obesity and insulin sensitivityWorth knowing
- rs1559085CAST · 96,742,998A;ANo summary available.Typical
- rs27044ERAP1 · 96,783,148C;Cnormal riskTypical
- rs17482078ERAP1 · 96,783,162C;C0.76x lower risk for spondylitisTypical
- rs10050860ERAP1 · 96,786,506T;THalf the risk (about 0.05%) of Ankylosing Spondylitis.Minor
- rs30187ERAP1 · 96,788,627T;T2x higher risk for Ankylosing Spondylitis.Worth knowing
- rs2287987ERAP1 · 96,793,832C;C0.71x lower risk for spondylitisTypical
- rs3734016ERAP1 · 96,803,761C;Ccommon on affy axiom dataTypical
- rs2549782ERAP1 · 96,895,296G;G1.6x increased risk for preeclampsia in most populationsMinor
- rs17408150ERAP1 · 96,903,554T;Tcommon on affy axiom dataTypical
- rs2303138LNPEP · 97,015,006A;A2.25x increased risk (0.2%) for Ankylosing Spondylitis.Worth knowing
- rs10515260ZCCHC5 · 97,740,844T;Tcommon genotypeTypical
- rs1174589099,380,064T;Tcommon genotypeTypical
- rs17167021CTD-2151A2.1 · 99,544,595A;Acommon genotypeTypical
- rs10067427100,006,343A;ANo summary available.Typical
- rs383830100,613,278T;T1.9x riskWorth knowing
- rs4702982100,655,944C;Ccommon in complete genomicsTypical
- rs17161553100,966,102T;Tcommon genotypeTypical
- rs13188771LOC105379102 · 101,612,841C;Ccommon on affy axiom dataTypical
- rs7705924LINC00491 · 102,611,094G;Ghigher odds of Crohn's diseaseWorth knowing
- rs7447447105,532,235C;Ccommon on affy axiom dataTypical
- rs10479334105,618,627T;Tcommon on affy axiom dataTypical
- rs13177718FER · 108,777,643C;CNo summary available.Typical
- rs36785109,998,341C;Ccommon in complete genomicsTypical
- rs7701890TMEM232 · 110,523,120A;A1x normalTypical
- rs17132261TMEM232 · 110,672,513C;Ccommon in complete genomicsTypical
- rs1837253TSLP · 111,066,174T;Treduced risk (0.73) for late-onset (adult) asthmaWorth knowing
- rs11241095WDR36 · 111,103,810A;Acommon/normalTypical
- rs1370967111,203,694G;Gcommon genotypeTypical
- rs10491334CAMK4 · 111,436,706C;Ccommon on affy axiom dataTypical
- rs379440EPB41L4A · 112,357,674T;Tcommon genotypeTypical
- rs587782557APC · 112,775,632-;ATFamilial Adenomatous PolyposisVery important
- rs2229992APC · 112,827,157G;TFamilial Adenomatous PolyposisVery important
- rs121913333APC · 112,838,220C;TFamilial Adenomatous PolyposisVery important
- rs1801155APC · 112,839,514A;Arisk of colon cancer and familial adenomatous polyposis (FAP) which usually progresses to malignancyVery important
- rs1801166APC · 112,839,543C;Cincreased colon cancer risk? significance is unclearImportant
- rs1804197APC · 112,844,212A;AIncreased risk of familial colorectal cancer and Asperger's syndromeWorth knowing
- rs6594681MCC · 113,104,244C;Ccommon in complete genomicsTypical
- rs17323670MCC · 113,244,593T;Tcommon genotypeTypical
- rs17136627LOC101927078 · 114,463,289C;Ccommon genotypeTypical
- rs400028LOC101927078 · 114,513,597T;Tcommon/normalTypical
- rs7702057COMMD10 · 116,392,141G;Gcommon in complete genomicsTypical
- rs7734156COMMD10 · 116,398,108G;Gcommon genotypeTypical
- rs12153048117,177,909C;Ccommon genotypeTypical
- rs25640HSD17B4 · 119,475,838C;GCarrier of a mutation for D-bifunctional protein deficiencyImportant
- rs1584468PRR16 · 120,601,996G;Gcommon genotypeTypical
- rs17147528121,270,010T;Tcommon in complete genomicsTypical
- rs1800449LOX · 122,077,513C;Ccommon in clinvarTypical
- rs11241713123,783,871C;CNo summary available.Typical
- rs6862844125,030,274A;Acommon in complete genomicsTypical
- rs2637496125,407,574C;Ccommon in complete genomicsTypical
- rs13182402ALDH7A1 · 126,582,456A;Acommon in complete genomicsTypical
- rs1546498126,697,272C;Ccommon genotypeTypical
- rs27388MEGF10 · 127,348,117A;AIncreased risk of developing schizophreniaWorth knowing
- rs12513840CCDC192 · 127,724,250A;Acommon genotypeTypical
- rs12523164CCDC192 · 127,726,279T;Tcommon genotypeTypical
- rs10463833CCDC192 · 127,786,620G;Gcommon genotypeTypical
- rs7722425CCDC192 · 127,790,070T;Tcommon genotypeTypical
- rs154001FBN2 · 128,349,443C;Ccommon in clinvarTypical
- rs246246ADAMTS19 · 129,721,066T;TNo summary available.Typical
- rs1355095MEIKIN · 131,913,076T;TnormalTypical
- rs3792876SLC22A4 · 132,301,616C;CNo summary available.Typical
- rs11568510SLC22A4 · 132,312,261A;Acommon in complete genomicsTypical
- rs2073838SLC22A4 · 132,313,529G;GNo summary available.Typical
- rs11568500SLC22A4 · 132,313,731G;Gcommon in complete genomicsTypical
- rs11568503LOC553103 · 132,327,296C;Ccommon in complete genomicsTypical
- rs272893SLC22A4 · 132,327,369C;Tcommon in complete genomicsTypical
- rs272889SLC22A4 · 132,329,685A;Gcommon in complete genomicsTypical
- rs272879SLC22A4 · 132,334,853C;Gcommon in complete genomicsTypical
- rs11568506SLC22A4 · 132,335,767G;Gcommon in complete genomicsTypical
- rs12777SLC22A4 · 132,335,969C;Ccommon in complete genomicsTypical
- rs1050152SLC22A4 · 132,340,627T;T2.1x increased risk of Crohn's diseaseWorth knowing
- rs2631367LOC553103 · 132,369,766G;GIncreased risk for Crohn's DiseaseTypical
- rs7731390SLC22A5 · 132,386,057C;Ccommon genotypeTypical
- rs11568514SLC22A5 · 132,392,510T;Tcommon in clinvarTypical
- rs28383481SLC22A5 · 132,393,688G;Gcommon in clinvarTypical
- rs6596075IBD5 · 132,406,536C;C2x risk of Crohn's diseaseTypical
- rs1003533C5orf56 · 132,419,959C;CNo summary available.Typical
- rs2188962IBD5 · 132,435,113C;Ccommon./normalTypical
- rs17166050RAD50 · 132,579,521G;Gcommon in clinvarTypical
- rs1800925TH2LCRR · 132,657,117C;Ccommon/normalTypical
- rs2243248IL4 · 132,672,952T;Tcommon in complete genomicsTypical
- rs2243250IL4 · 132,673,462C;T0.6x decreased risk for myocardial infarction if younger than 50Worth knowing
- rs2070874IL4 · 132,674,018C;CNo summary available.Typical
- rs17166496FSTL4 · 133,293,192C;C1.1x risk for type-1 diabetesTypical
- rs5742913TCF7 · 134,115,992C;CNo summary available.Typical
- rs17653687TCF7 · 134,132,309A;ANo summary available.Typical
- rs479632PITX1 · 135,028,828C;Ccommon in clinvarTypical
- rs6596189C5orf66 · 135,032,479T;TNo summary available.Worth knowing
- rs2069885IL9 · 135,892,476G;Gcommon on affy axiom dataTypical
- rs2069868IL9 · 135,897,277G;Gcommon in complete genomicsTypical
- rs17170899SPOCK1 · 137,040,361C;Ccommon in complete genomicsTypical
- rs13357391SPOCK1 · 137,105,393C;Cslightly earlier age at menarcheTypical
- rs1859345SPOCK1 · 137,111,731C;Cslightly earlier age at menarcheTypical
- rs6890689MYOT · 137,870,871A;Acommon in clinvarTypical
- rs28363394CTNNA1 · 138,812,250C;Ccommon in clinvarTypical
- rs2547547HDAC3 · 141,626,120A;Acommon in complete genomicsTypical
- rs251177FCHSD1 · 141,647,317C;Csomewhat higher risk for prostate cancerTypical
- rs4324715142,289,942C;C>1.5x increased testicular cancer risk for menMinor
- rs4624820142,302,223A;Aincreased testicular cancer risk for menTypical
- rs6897876142,308,074C;Cslight increase in testicular cancer risk for menMinor
- rs17577085142,484,039T;Tcommon in complete genomicsTypical
- rs6198NR3C1 · 143,278,056T;Tcommon in clinvarTypical
- rs6193NR3C1 · 143,279,701T;Tcommon in clinvarTypical
- rs6196NR3C1 · 143,281,925A;Acommon in complete genomicsTypical
- rs2918419NR3C1 · 143,342,788T;Tcommon in complete genomicsTypical
- rs9324921NR3C1 · 143,388,175C;Ccommon genotypeTypical
- rs56149945NR3C1 · 143,399,752T;Tcommon in clinvarTypical
- rs6195NR3C1 · 143,399,752T;TNo summary available.Typical
- rs6190NR3C1 · 143,400,772C;Ccommon in complete genomicsTypical
- rs6189NR3C1 · 143,400,774C;Ccommon in complete genomicsTypical
- rs26160145,353,893T;Tcommon in complete genomicsTypical
- rs10074645145,585,822C;Ccommon in complete genomicsTypical
- rs10515552PRELID2 · 145,659,268T;Tcommon in complete genomicsTypical
- rs4705423146,535,510T;Tcommon in complete genomicsTypical
- rs4705038STK32A · 147,354,035C;Ccommon in complete genomicsTypical
- rs17107315SPINK1 · 147,828,115G;Grisk of pancreatitisVery important
- rs2303063SPINK5 · 148,100,464G;Gcommon in clinvarTypical
- rs2303064SPINK5 · 148,100,517G;Gcommon in clinvarTypical
- rs2303067SPINK5 · 148,101,392A;A1.8x riskTypical
- rs3777134SPINK5 · 148,118,456G;Gcommon in clinvarTypical
- rs9325113148,718,440C;Ccommon in complete genomicsTypical
- rs1042713ADRB2 · 148,826,877A;A1.7x increased risk that pediatric inhaler use may make asthma worseMinor
- rs17334242ADRB2 · 148,826,877A;ANo summary available.Typical
- rs1042714ADRB2 · 148,826,910C;CnormalTypical
- rs1800888ADRB2 · 148,827,322T;Tincreased risk of coronary artery diseaseWorth knowing
- rs10044242AFAP1L1 · 149,326,736C;Ccommon genotypeTypical
- rs9285640PPARGC1B · 149,762,504G;Gcommon genotypeTypical
- rs741581PPARGC1B · 149,823,222G;Gcommon in complete genomicsTypical
- rs7732671PPARGC1B · 149,832,680G;Gcommon in clinvarTypical
- rs30832SLC26A2 · 149,981,314T;Tcommon in clinvarTypical
- rs10079250CSF1R · 150,070,569T;Tcommon in clinvarTypical
- rs13153971SLC6A7 · 150,201,758C;C1.58x higher risk of Asthma.Worth knowing
- rs2255796TCOF1 · 150,371,783A;Gcommon in complete genomicsTypical
- rs15251TCOF1 · 150,396,669C;Ccommon in clinvarTypical
- rs13361189150,843,825C;C2.6x increased risk for Crohn's diseaseWorth knowing
- rs10065172IRGM · 150,848,436C;Ccommon in complete genomicsTypical
- rs4958847IRGM · 150,860,025A;A2.6x increased risk for Crohn's diseaseWorth knowing
- rs1000113IRGM · 150,860,514C;CnormalTypical
- rs11747270IRGM · 150,879,305A;Acommon in complete genomicsTypical
- rs7714584IRGM · 150,890,858A;Acommon in complete genomicsTypical
- rs3805435GPX3 · 151,021,735T;Tcommon in complete genomicsTypical
- rs4958881TNIP1 · 151,070,675T;Tcommon/normalTypical
- rs17728338ANXA6 · 151,098,757G;Gcommon in complete genomicsTypical
- rs11960458ANXA6 · 151,100,959C;Ccommon in complete genomicsTypical
- rs153477GM2A · 151,259,848A;Acommon in clinvarTypical
- rs153478GM2A · 151,259,878A;Acommon in clinvarTypical
- rs17504622153,274,919C;Ccommon genotypeTypical
- rs689732LOC107986464 · 153,960,408C;Ccommon in complete genomicsTypical
- rs13186787GALNT10 · 154,347,209A;Acommon in complete genomicsTypical
- rs11134474SGCD · 155,775,518A;Acommon in complete genomicsTypical
- rs17053082SGCD · 155,967,220C;Ccommon genotypeTypical
- rs157350SGCD · 156,712,558A;Acommon in complete genomicsTypical
- rs11135380SGCD · 156,755,037G;Gcommon genotypeTypical
- rs11740562ADAM19 · 157,515,277A;Acommon on affy axiom dataTypical
- rs2149954LOC101927697 · 158,393,594T;Tslight association with longer life (longevity)Minor
- rs3181224LOC105377683 · 159,313,842A;ANo summary available.Typical
- rs1368439IL12B · 159,315,006G;Gcommon in clinvarTypical
- rs3212227IL12B · 159,315,942G;TSignificantly increased risk of developing cervical cancerWorth knowing
- rs3213120IL12B · 159,316,100C;Ccommon in complete genomicsTypical
- rs3213119IL12B · 159,316,780G;GNo summary available.Typical
- rs3213094IL12B · 159,323,761T;T0.79x risk for psoriasisTypical
- rs2546890LOC285626 · 159,332,892A;AHigher risk of multiple sclerosisMinor
- rs7709212LOC285626 · 159,337,169C;C0.82x risk of Psioriasis in ChineseTypical
- rs6887695159,395,637C;CnormalTypical
- rs12188300159,402,519A;Acommon on affy axiom dataTypical
- rs10866713159,491,886G;Gcommon in complete genomicsTypical
- rs2277920MIR3142HG · 160,468,698T;Tcommon in complete genomicsTypical
- rs2961920MIR146A · 160,484,499A;ANo summary available.Typical
- rs2910164MIR146A · 160,485,411C;Chigher cancer risk ? (ambiguous flip)Worth knowing
- rs2229944GABRB2 · 161,294,312G;Gcommon in clinvarTypical
- rs1816071GABRB2 · 161,332,949A;GNo summary available.Typical
- rs2279020GABRA1 · 161,895,883G;Gcommon in clinvarTypical
- rs2290732GABRA1 · 161,897,892A;Acommon in clinvarTypical
- rs299284HMMR · 163,469,644C;Ccommon on affy axiom dataTypical
- rs10515860HMMR · 163,490,702G;Gcommon in complete genomicsTypical
- rs6556756LOC105377703 · 164,462,274T;Tcommon on affy axiom dataTypical
- rs9313296165,950,694G;Gcommon in complete genomicsTypical
- rs2122554166,530,081G;Gcommon in complete genomicsTypical
- rs3853240LOC105377706 · 166,891,185A;Acommon in complete genomicsTypical
- rs17404956166,962,488A;Acommon in complete genomicsTypical
- rs2937573TENM2 · 167,044,193G;G1.2x more sensitive to chewing soundsTypical
- rs2973662TENM2 · 167,783,467G;GNo summary available.Typical
- rs17070145WWC1 · 168,418,786C;Creduced memory abilitiesWorth knowing
- rs12514426WWC1 · 168,466,703G;Gcommon in complete genomicsTypical
- rs749318706WWC1 · 168,467,849C;TDe novo mutation seen in a Tourette syndrome proband; implied but unproven associationImportant
- rs11739136KCNMB1 · 170,383,792C;Ccommon in clinvarTypical
- rs11957313KCNIP1 · 170,523,390G;Gcommon in complete genomicsTypical
- rs12513649173,045,049C;Ccommon genotypeTypical
- rs373863828CREBRF · 173,108,771A;G1.35x increased obesity risk, at least for SamoansMinor
- rs703752NKX2-5 · 173,232,508C;Ccommon in clinvarTypical
- rs3729753NKX2-5 · 173,232,938C;Ccommon in complete genomicsTypical
- rs28936670NKX2-5 · 173,235,011G;Gcommon in clinvarTypical
- rs2277923NKX2-5 · 173,235,021T;Tcommon in clinvarTypical
- rs3095870NKX2-5 · 173,236,451C;T1.7x increased risk for SLE (lupus)Typical
- rs1106693CPEB4 · 173,925,760A;Acommon genotypeTypical
- rs17763373CPEB4 · 173,932,328A;ANo summary available.Typical
- rs4242182MSX2 · 174,729,165C;CNo summary available.Typical
- rs686DRD1 · 175,441,697G;GNo summary available.Typical
- rs155417DRD1 · 175,441,837C;Ccommon in complete genomicsTypical
- rs1799914DRD1 · 175,442,902C;Ccommon in complete genomicsTypical
- rs4532DRD1 · 175,443,147C;CNo summary available.Typical
- rs5326DRD1 · 175,443,193C;Tpossible psychiatric risksMinor
- rs265981DRD1 · 175,443,899A;ANo summary available.Typical
- rs2067474HRH2 · 175,682,216G;Gcommon in complete genomicsTypical
- rs351855FGFR4 · 177,093,242A;A2x increased prostate cancer risk; among breast cancer patients, herceptin is less effectiveWorth knowing
- rs2011077FGFR4 · 177,094,455C;CIn Japanese, 6.2x increased risk of developing prostate cancer, a 3x increased risk of developing BPH, and a 5.5x increased risk of developing metastatic prostate cancerImportant
- rs28932177NSD1 · 177,210,470G;Gcommon in clinvarTypical
- rs28932178NSD1 · 177,210,575C;CNo summary available.Typical
- rs11746443RGS14 · 177,371,305A;A1.19x risk of kidney stone in JapaneseTypical
- rs1801020F12 · 177,409,531A;G1.31x increased risk of heart diseaseMinor
- rs28937869B4GALT7 · 177,608,994T;TEhlers-Danlos syndromeVery important
- rs1054480ADAMTS2 · 179,113,974G;Gcommon in clinvarTypical
- rs901254ADAMTS2 · 179,272,310C;Ccommon genotypeTypical
- rs730012LTC4S · 179,793,637A;Acommon in clinvarTypical
- rs2291418MGAT4B · 179,798,324G;Gcommon in complete genomicsTypical
- rs10464059180,367,208A;AIncreased risk of developing Parkinson's DiseaseWorth knowing
- rs307826FLT4 · 180,624,003T;Tcommon on affy axiom dataTypical
- rs12517906LOC100289003 · 180,743,819C;Ccommon on affy axiom dataTypical
- rs655601MGAT1 · 180,799,673A;ANo 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.