Chromosome 10
422 well-documented SNPs on chromosome 10, in order of position (GRCh38).
- rs10794720WDR37 · 1,110,225C;Ccommon in complete genomicsTypical
- rs6560749ADARB2 · 1,634,336G;Gcommon in complete genomicsTypical
- rs93293002,747,402C;Ccommon genotypeTypical
- rs6602024PFKP · 3,113,045A;A1-3 body mass index units heavier on averageTypical
- rs3750861KLF6 · 3,782,241C;Ccommon in complete genomicsTypical
- rs66017643,820,350C;C1.52x increased risk of developing Crohn's diseaseWorth knowing
- rs112523944,198,678G;Gcommon genotypeTypical
- rs124160004,797,975A;ANeanderthal geneWorth knowing
- rs2290349AKR1E2 · 4,839,743A;Acommon in complete genomicsTypical
- rs17133762AKR1E2 · 4,846,947C;Ccommon in complete genomicsTypical
- rs112528454,951,623C;Ccommon in complete genomicsTypical
- rs17134592AKR1C4 · 5,218,719C;Ccommon on affy axiom dataTypical
- rs79115005,995,763C;Ccommon in complete genomicsTypical
- rs12722605IL2RA · 6,011,200T;Tcommon in complete genomicsTypical
- rs2104286IL2RA · 6,057,082C;Cprotective minor allele, slightly reducing risk for MS & RAMinor
- rs3118470IL2RA · 6,059,750T;TNo summary available.Typical
- rs12722489IL2RA · 6,060,049C;Ta slight increase in risk of developing multiple sclerosisTypical
- rs12722486IL2RA · 6,061,799C;Ccommon genotypeTypical
- rs122513076,081,532C;Ccommon in complete genomicsTypical
- rs500766PRKCQ · 6,508,628C;Ccommon/normalTypical
- rs1244414ATP5C1 · 7,794,141C;Ccommon/normalTypical
- rs4143094GATA3 · 8,047,173T;Thigher (by 39%) risk for colorectal cancer correlated with consumption of processed meatsImportant
- rs3824662GATA3 · 8,062,245C;Ccommon/normalTypical
- rs105083438,108,750C;Ccommon in complete genomicsTypical
- rs112556158,282,926T;Tcommon genotypeTypical
- rs105083728,930,055G;Gcommon in complete genomicsTypical
- rs122473979,321,914A;Acommon genotypeTypical
- rs11256676CELF2 · 10,559,897A;Acommon genotypeTypical
- rs1291846CELF2 · 11,065,232A;ANo summary available.Typical
- rs523747OPTN · 13,124,076G;GNo summary available.Typical
- rs11259096MIR1265 · 14,436,619T;Tcommon in complete genomicsTypical
- rs2278871CDNF · 14,819,402C;Ccommon in complete genomicsTypical
- rs1901650CDNF · 14,822,888T;Tcommon in complete genomicsTypical
- rs11259365CDNF · 14,834,528G;Gcommon in complete genomicsTypical
- rs7077361ITGA8 · 15,519,544T;Tcommon on affy axiom dataTypical
- rs2298033ITGA8 · 15,607,711G;GNo summary available.Typical
- rs7895372ITGA8 · 15,677,622C;Ccommon in complete genomicsTypical
- rs2297882FAM188A · 15,860,304A;Acommon in complete genomicsTypical
- rs1050850316,257,952C;Ccommon on affy axiom dataTypical
- rs7893395CUBN · 16,863,501C;Ccommon in complete genomicsTypical
- rs1801239CUBN · 16,877,053T;Tcommon on affy axiom dataTypical
- rs10508517CUBN · 16,955,892G;GNo summary available.Typical
- rs1801222CUBN · 17,114,152A;Acommon in clinvarTypical
- rs11254385CUBN · 17,129,763C;Ccommon in clinvarTypical
- rs359312ST8SIA6 · 17,346,144C;Ccommon in complete genomicsTypical
- rs2477664MRC1 · 17,833,817T;Tcommon in complete genomicsTypical
- rs1766153818,108,318G;Gcommon in complete genomicsTypical
- rs12258967CACNB2 · 18,439,030C;Gcommon in complete genomicsTypical
- rs2228645NSUN6 · 18,539,442C;Ccommon in clinvarTypical
- rs1326986C10orf112 · 19,640,584T;Tcommon in complete genomicsTypical
- rs1692062420,521,596T;Tcommon in complete genomicsTypical
- rs12770228C10orf114 · 21,494,705A;A2x increased risk for meningiomaWorth knowing
- rs11012732MLLT10 · 21,541,175G;G2x increased risk for meningiomaWorth knowing
- rs1181444822,026,914A;Acommon genotypeTypical
- rs16923476LOC105376454 · 23,569,282G;Gcommon genotypeTypical
- rs11014002KIAA1217 · 24,275,724C;Ccommon in complete genomicsTypical
- rs16924573KIAA1217 · 24,315,964G;GNo summary available.Typical
- rs17558301GPR158 · 25,591,530C;Ccommon genotypeTypical
- rs1277553525,629,950C;CNo summary available.Typical
- rs16926523MYO3A · 26,005,899G;Gcommon genotypeTypical
- rs1334893PTCHD3 · 27,404,376A;ANo summary available.Typical
- rs4317882MPP7 · 28,135,248G;Gcommon in complete genomicsTypical
- rs11006923MPP7 · 28,216,015T;Tcommon in complete genomicsTypical
- rs2368392SVIL · 29,545,074G;GNo summary available.Typical
- rs12416605SVIL · 29,602,331C;CNo summary available.Typical
- rs2484992LOC101929352 · 31,223,169C;Ccommon genotypeTypical
- rs2484990LOC101929352 · 31,226,203C;Ccommon genotypeTypical
- rs7081678LOC101929951 · 31,701,695G;GNo summary available.Typical
- rs11009175LOC101929475 · 33,005,847G;Gcommon on affy axiom dataTypical
- rs2228638NRP1 · 33,186,354C;CNo summary available.Typical
- rs563507PARD3 · 34,529,060G;Gcommon on affy axiom dataTypical
- rs1101029035,771,381A;ANormalTypical
- rs1148259ANKRD30A · 37,219,522C;Clowest sphingomyelin ratiosTypical
- rs747489637,693,169C;Ccommon on affy axiom dataTypical
- rs1181506637,742,055G;GNo summary available.Typical
- rs214299142,845,657T;Tcommon on affy axiom dataTypical
- rs17857727RET · 43,100,520G;GNo summary available.Typical
- rs1800858RET · 43,100,520A;AnormalTypical
- rs1800860RET · 43,111,239G;GNormal sized kidneys as newbornsMinor
- rs9282834RET · 43,111,408G;Gcommon in clinvarTypical
- rs75076352RET · 43,114,500T;Tcommon in clinvarTypical
- rs1799939RET · 43,114,671G;Gcommon in complete genomicsTypical
- rs2472737RET · 43,120,057G;Gcommon in clinvarTypical
- rs1800863RET · 43,120,185C;Ccommon in complete genomicsTypical
- rs74799832RET · 43,121,968C;TMultiple Endocrine Neoplasia IIAVery important
- rs17158558RET · 43,124,887C;CnormalTypical
- rs2075912RET · 43,126,769T;Tcommon in clinvarTypical
- rs3026785RET · 43,130,238C;Cmay be protective against Hirschsprung diseaseTypical
- rs9326506ZNF239 · 43,573,110A;ANo summary available.Typical
- rs1715492944,029,227C;Ccommon in complete genomicsTypical
- rs50112044,258,419T;Tcommon, but >1.3x increased risk for heart diseaseMinor
- rs174604844,280,376T;T0.85 decreased risk for coronary heart diseaseWorth knowing
- rs2146807CXCL12 · 44,318,290T;Tcommon in complete genomicsTypical
- rs1804429CXCL12 · 44,370,393A;Acommon in complete genomicsTypical
- rs1801157CXCL12 · 44,372,809T;T1.4x higher risk for breast cancerMinor
- rs148059744,665,661C;CNo summary available.Typical
- rs7911712LOC220980 · 44,824,206G;Gcommon on affy axiom dataTypical
- rs2228064ALOX5 · 45,382,602G;Gcommon in complete genomicsTypical
- rs2228065ALOX5 · 45,425,058G;Gcommon in complete genomicsTypical
- rs2279434MARCH8 · 45,459,616C;Ccommon on affy axiom dataTypical
- rs901683MARCH8 · 45,470,974G;Gcommon genotypeTypical
- rs7085433TIMM23 · 46,002,468G;Gcommon on affy axiom dataTypical
- rs10740051NCOA4 · 46,025,670G;Gcommon in complete genomicsTypical
- rs7904463MSMB · 46,036,353C;Ccommon in complete genomicsTypical
- rs10993994MSMB · 46,046,326T;Tincreased prostate cancer risk (odds ratio 1.6)Worth knowing
- rs10857636WDFY4 · 48,777,065C;Ccommon in complete genomicsTypical
- rs3849150WDFY4 · 48,901,178C;CNo summary available.Typical
- rs483850849,353,462C;Ccommon in complete genomicsTypical
- rs4253208ERCC6 · 49,470,676G;Gcommon in clinvarTypical
- rs4253196ERCC6 · 49,473,613T;Tcommon in clinvarTypical
- rs4253132ERCC6 · 49,493,110G;Gcommon in clinvarTypical
- rs3793784ERCC6 · 49,539,493C;G1.5x risk for ARMDWorth knowing
- rs733722CHAT · 49,608,897C;Cno positive effect of AChE inhibitors for Alzheimer's patientsTypical
- rs1880676CHAT · 49,616,071G;Gcommon in clinvarTypical
- rs3810950CHAT · 49,616,573G;Gcommon in clinvarTypical
- rs8178990CHAT · 49,622,125C;Ccommon in complete genomicsTypical
- rs2177369CHAT · 49,635,683G;G1.5x increased risk for Alzheimer's diseaseMinor
- rs4838544CHAT · 49,648,606A;Acommon in complete genomicsTypical
- rs2043556PRKG1 · 51,299,646A;ANo summary available.Typical
- rs1569198DKK1 · 52,316,511A;Acommon/normalTypical
- rs1881747LOC105378305 · 52,573,815C;C1.24x increased risk for LOADTypical
- rs10824792MBL2 · 52,766,446C;Ccommon in clinvarTypical
- rs1800451MBL2 · 52,771,466T;Tmannose binding deficiency but of low clinical importanceMinor
- rs1800450MBL2 · 52,771,475T;Tmannose binding deficiency but of low clinical importanceMinor
- rs5030737MBL2 · 52,771,482A;Amannose binding deficiency but of low clinical importanceMinor
- rs7096206MBL2 · 52,771,925C;Ccommon/normalTypical
- rs1225683053,624,983C;Ccommon in complete genomicsTypical
- rs2135720PCDH15 · 53,995,731C;Ccommon in clinvarTypical
- rs10825264PCDH15 · 54,188,194T;Tcommon in complete genomicsTypical
- rs16905691PCDH15 · 54,190,139T;Tcommon in complete genomicsTypical
- rs4935502PCDH15 · 54,195,684T;Tcommon in complete genomicsTypical
- rs10825269PCDH15 · 54,195,850C;Ccommon in clinvarTypical
- rs16906916PCDH15 · 55,089,225A;Acommon in complete genomicsTypical
- rs1082599257,188,447G;GIncreased high myopia riskWorth knowing
- rs3586632657,557,163C;Ccommon in complete genomicsTypical
- rs708859157,964,643A;Acommon genotypeTypical
- rs2790232IPMK · 58,225,910C;Ccommon genotypeTypical
- rs1937TFAM · 58,385,582G;Gcommon on affy axiom dataTypical
- rs7085387LOC105378316 · 58,444,842A;GNo summary available.Typical
- rs11006263BICC1 · 58,795,818A;ANo summary available.Typical
- rs1100646459,386,824T;Tcommon genotypeTypical
- rs12356193SLC16A9 · 59,653,595A;Acommon in complete genomicsTypical
- rs7094971SLC16A9 · 59,689,806A;Acommon in complete genomicsTypical
- rs227942060,022,189G;G0.79x decreased risk for LOADTypical
- rs28932171ANK3 · 60,071,532T;Tcommon in clinvarTypical
- rs11599164ANK3 · 60,072,226G;Gcommon in clinvarTypical
- rs17208576ANK3 · 60,074,815G;Gcommon in clinvarTypical
- rs3750800ANK3 · 60,108,958C;Ccommon in clinvarTypical
- rs10994336ANK3 · 60,420,054C;T1.45x increased odds of developing bipolar disorderWorth knowing
- rs4948418ANK3 · 60,425,736C;CNo summary available.Typical
- rs10994397ANK3 · 60,519,366C;Ccommon in complete genomicsTypical
- rs1530440C10orf107 · 61,764,833C;Ccommon in complete genomicsTypical
- rs751891LOC107984237 · 61,781,965G;Gcommon in complete genomicsTypical
- rs10821936ARID5B · 61,963,818C;CHigher risk of childhood acute lymphoblastic leukemiaWorth knowing
- rs10994994ARID5B · 61,987,926T;Tcommon in complete genomicsTypical
- rs7089424ARID5B · 61,992,400G;Gmoderately (~4x) increased risk for acute lymphoblastic leukemiaWorth knowing
- rs7089814ZNF365 · 62,427,805C;C1.2 breast size (bigger breast size)Worth knowing
- rs2393903ZNF365 · 62,620,576T;TnormalTypical
- rs7076156ZNF365 · 62,655,424A;ANo summary available.Worth knowing
- rs1076165962,685,804A;G1.2x risk of Crohn's diseaseMinor
- rs2295814EGR2 · 62,811,516G;Gcommon in complete genomicsTypical
- rs10995315EGR2 · 62,814,811G;Gcommon in complete genomicsTypical
- rs10995356LOC107984012 · 62,896,153A;ALikely more reward dependentMinor
- rs10995485JMJD1C · 63,267,098G;Gcommon genotypeTypical
- rs938036LOC105378332 · 63,898,984C;Ccommon genotypeTypical
- rs7900909LOC105378334 · 64,688,715T;Tcommon in complete genomicsTypical
- rs12251332CTNNA3 · 66,206,816G;Gcommon genotypeTypical
- rs16922827CTNNA3 · 66,325,595T;Tcommon in complete genomicsTypical
- rs10762058CTNNA3 · 66,328,750G;Gcommon in complete genomicsTypical
- rs2306402CTNNA3 · 67,175,727C;C1.18x increased risk for late-onset Alzheimer's diseaseWorth knowing
- rs789583367,863,299A;Acommon in complete genomicsTypical
- rs3758391SIRT1 · 67,883,584T;TIncreased longevity. Less mental decline with age.Worth knowing
- rs3740051SIRT1 · 67,884,201A;ANo summary available.Typical
- rs2273773SIRT1 · 67,906,841T;Tcommon in complete genomicsTypical
- rs4746720SIRT1 · 67,917,073T;Tcommon in complete genomicsTypical
- rs10823116HERC4 · 67,923,688A;Acommon in complete genomicsTypical
- rs12571093LOC100128041 · 68,259,614A;Aancestral Neanderthal allele (homozygote)Minor
- rs5030882TET1 · 68,692,714C;CNo summary available.Minor
- rs10998466STOX1 · 68,866,673A;Acommon genotypeTypical
- rs1341667STOX1 · 68,882,104T;Tcommon in clinvarTypical
- rs10509305STOX1 · 68,885,620C;Cfetuses with this genotype may cause maternal pre-eclampsiaImportant
- rs2017305DDX50 · 68,952,306A;ANo summary available.Typical
- rs10998624SUPV3L1 · 69,180,045G;Gcommon genotypeTypical
- rs4536103NEUROG3 · 69,572,448A;Acommon in clinvarTypical
- rs7653SAR1A · 70,150,560A;Acommon/normalTypical
- rs4747011LRRC20 · 70,354,622C;Ccommon genotypeTypical
- rs1904589NODAL · 70,435,683T;Tcommon in clinvarTypical
- rs885822PRF1 · 70,598,821G;Gcommon in clinvarTypical
- rs28933375PRF1 · 70,598,966C;CFamilial Hemophagocytic Lymphohistiocytosis and LymphomaVery important
- rs17600642ADAMTS14 · 70,703,238C;Ccommon in complete genomicsTypical
- rs1276122470,767,761G;Gcommon in complete genomicsTypical
- rs2252996SLC29A3 · 71,356,185G;Gcommon in clinvarTypical
- rs1084004SLC29A3 · 71,362,188T;Tcommon in clinvarTypical
- rs141721071,376,162G;G0.88x risk of vitiligo in ChineseTypical
- rs3752752CDH23 · 71,695,444T;Tcommon in clinvarTypical
- rs11592462CDH23 · 71,790,360C;Ccommon in clinvarTypical
- rs11000019PSAP · 71,831,773G;Gcommon genotypeTypical
- rs4148941CHST3 · 72,009,234A;CSlightly higher (1.5) risk for lumbar disc disease (?)Minor
- rs4148943CHST3 · 72,009,749C;Ccommon in clinvarTypical
- rs4148945CHST3 · 72,009,832C;Ccommon in clinvarTypical
- rs4148947CHST3 · 72,010,359T;Tcommon in clinvarTypical
- rs4148950CHST3 · 72,011,948G;Gcommon in clinvarTypical
- rs1871450CHST3 · 72,012,256G;Gcommon in clinvarTypical
- rs730720CHST3 · 72,013,004C;Ccommon in clinvarTypical
- rs12418CHST3 · 72,013,256G;Gcommon in clinvarTypical
- rs2227564PLAU · 73,913,343T;Tcommon in clinvarTypical
- rs4065PLAU · 73,916,706C;Ccommon in clinvarTypical
- rs7919006DUPD1 · 75,049,002C;Ccommon in complete genomicsTypical
- rs2043090C10orf11 · 75,538,851A;ANo summary available.Typical
- rs2116830KCNMA1 · 76,886,778G;Gcommon on affy axiom dataTypical
- rs1248696DLG5 · 77,856,847C;Ccommon on affy axiom dataTypical
- rs1051246SFTPD · 79,938,062A;Acommon in clinvarTypical
- rs3088308SFTPD · 79,938,112A;Acommon in clinvarTypical
- rs911887SFTPD · 79,941,767C;Tcommon in complete genomicsTypical
- rs2243639SFTPD · 79,941,966T;Tcommon in clinvarTypical
- rs721917SFTPD · 79,946,568A;Acommon in clinvarTypical
- rs12219080SFTPD · 79,949,523C;Ccommon in complete genomicsTypical
- rs7091565ANXA11 · 80,153,805C;CnormalTypical
- rs1049550ANXA11 · 80,166,946G;G1.6x increased risk of sarcoidosisTypical
- rs2993763MAT1A · 80,273,838G;Gcommon in clinvarTypical
- rs58851781,393,490C;Ccommon in complete genomicsTypical
- rs4933824NRG3 · 82,059,369G;Gcommon in complete genomicsTypical
- rs12098564LINC01519 · 85,193,571A;Acommon genotypeTypical
- rs7910620GRID1 · 86,087,202C;Ccommon in complete genomicsTypical
- rs2675703OPN4 · 86,654,812C;Ccommon on affy axiom dataTypical
- rs966422287,578,876C;Ccommon in complete genomicsTypical
- rs1060500116PTEN · 87,925,524C;GCowden syndrome (PTEN hamartoma tumor syndrome) mutationVery important
- rs701848PTEN · 87,966,988T;Tcommon in clinvarTypical
- rs121434528ACTA2 · 88,939,543A;GThoracic aortic aneurysm and dissection (TAAD) mutationVery important
- rs2234978FAS · 89,012,072T;Tcommon in clinvarTypical
- rs1468063FAS · 89,015,534C;Ccommon in clinvarTypical
- rs1131706LIPA · 89,213,919A;Acommon in clinvarTypical
- rs3802656LIPA · 89,215,892G;Gcommon in clinvarTypical
- rs1051338LIPA · 89,247,603T;Tcommon in clinvarTypical
- rs3740030SLC16A12 · 89,462,530A;Acommon in complete genomicsTypical
- rs2209972MARK2P9 · 92,419,271C;Chigher risk for PCOS?Typical
- rs7910977IDE · 92,450,119C;T~0.80x (lower) risk for late onset Alzheimer's diseaseMinor
- rs4646958IDE · 92,454,602T;Tcommon in complete genomicsTypical
- rs3781239IDE · 92,458,040C;Ccommon in complete genomicsTypical
- rs6583817IDE · 92,487,490C;T~0.80x (lower) risk for late onset Alzheimer's diseaseMinor
- rs7895832IDE · 92,516,769A;Acommon in complete genomicsTypical
- rs17107734IDE · 92,545,660C;Ccommon in complete genomicsTypical
- rs4646954IDE · 92,574,070G;Gcommon in complete genomicsTypical
- rs3758505IDE · 92,575,021A;Acommon in complete genomicsTypical
- rs111187592,703,125T;T1x normal risk of T2DTypical
- rs792383792,722,160G;G3.2x risk for T2DWorth knowing
- rs640090PDE6C · 93,632,828C;Ccommon genotypeTypical
- rs17417407PLCE1 · 94,171,330G;Gcommon in clinvarTypical
- rs11187837PLCE1 · 94,276,223T;Tcommon in complete genomicsTypical
- rs2274224PLCE1 · 94,279,840G;Gcommon in clinvarTypical
- rs3765524PLCE1 · 94,298,541C;Ccommon in clinvarTypical
- rs2274223PLCE1 · 94,306,584G;G1.9x increased risk for stomach & esophageal cancer (seen in Han Chinese)Worth knowing
- rs3203713PLCE1 · 94,327,971A;Acommon in clinvarTypical
- rs11187870PLCE1 · 94,328,109G;Gcommon in complete genomicsTypical
- rs12777823LOC100130970 · 94,645,745A;AAvoid Plavix, higher risk for adverse cardiovascular events. CYP2C19 poor metabolizer.Important
- rs3814637CYP2C19 · 94,761,288C;CNo summary available.Typical
- rs12248560CYP2C19 · 94,761,900C;TCYP2C19*17 ultra fast metabolizer; drug metabolism effects; also 0.77x decreased breast cancer riskWorth knowing
- rs28399504CYP2C19 · 94,762,706G;Gpoor metabolizerWorth knowing
- rs4986893CYP2C19 · 94,780,653A;Apoor metabolizer of several commonly prescribed drugsWorth knowing
- rs6413438CYP2C19 · 94,781,858T;TCYP2C19*10 homozygoteImportant
- rs4244285CYP2C19 · 94,781,859A;Apoor metabolizer of several popular medicines; patients prescribed Plavix get less benefit, and have higher risk for adverse cardiovascular eventsVery important
- rs3758580CYP2C19 · 94,842,865C;Ccommon/normalTypical
- rs3758581CYP2C19 · 94,842,866A;ACYP2C19 V331I homozygoteTypical
- rs17879685CYP2C19 · 94,849,995C;CnormalTypical
- rs1799853CYP2C9 · 94,942,290T;T~ 40% reduction in warfarin metabolism, greater NSAID riskWorth knowing
- rs12572351CYP2C9 · 94,943,463G;GNo summary available.Typical
- rs7089580CYP2C9 · 94,945,466A;ANo summary available.Typical
- rs4086116CYP2C9 · 94,947,445C;CNo summary available.Typical
- rs2256871CYP2C9 · 94,949,217G;GCYP2C9*9 homozygoteTypical
- rs9332130CYP2C9 · 94,949,280A;AnormalTypical
- rs9332146CYP2C9 · 94,962,487G;Gcommon in complete genomicsTypical
- rs4917639CYP2C9 · 94,965,778A;Acommon in clinvarTypical
- rs10509680CYP2C9 · 94,974,582G;TNo summary available.Important
- rs28371685CYP2C9 · 94,981,224T;TCYP2C9*11 homozygoteWorth knowing
- rs1057909CYP2C9 · 94,981,294G;GCYP2C9_42612A>G homozygoteVery important
- rs1057910CYP2C9 · 94,981,296C;CCYP2C9*3 homozygote; average 80% reduction in warfarin metabolism; reduced metabolism of number of other drugsVery important
- rs17847042CYP2C9 · 94,981,296A;ANo summary available.Typical
- rs1934968CYP2C9 · 94,982,060G;Gcommon in complete genomicsTypical
- rs2017319CYP2C9 · 94,988,878C;CnormalTypical
- rs1057911CYP2C9 · 94,988,980A;Tcarrier of one CYP2C9_50298A>T alleleImportant
- rs9332239CYP2C9 · 94,989,020C;CnormalTypical
- rs2185570LOC107984256 · 94,991,513T;Tcommon on affy axiom dataTypical
- rs10509681CYP2C8 · 95,038,992C;C>1.81x risk of GI bleeding with some NSAID drugsWorth knowing
- rs11572103CYP2C8 · 95,058,349T;Tcommon in complete genomicsTypical
- rs1058930CYP2C8 · 95,058,362G;GnormalTypical
- rs11572080CYP2C8 · 95,067,273T;T>1.81x risk of GI bleeding with NSAID drugsWorth knowing
- rs2071426CYP2C8 · 95,068,566T;Tcommon in clinvarTypical
- rs6584066DNTT · 96,318,482G;Gcommon in complete genomicsTypical
- rs7895244PIK3AP1 · 96,672,946T;Tcommon genotypeTypical
- rs2297644HOGA1 · 97,599,982T;Tcommon/normalTypical
- rs35077384ZFYVE27 · 97,749,494G;Gcommon in clinvarTypical
- rs508001CRTAC1 · 97,995,216A;Acommon in complete genomicsTypical
- rs577969HPSE2 · 98,531,419C;Ccommon genotypeTypical
- rs12570188HPSE2 · 99,095,945C;Ccommon genotypeTypical
- rs440976499,524,480G;Gnormal risk of Crohn's diseaseTypical
- rs10883365LINC01475 · 99,528,007G;G1.62x increased risk for developing Crohn's diseaseWorth knowing
- rs1119016499,591,947A;Acommon/normalTypical
- rs911541ENTPD7 · 99,673,635A;AnormalTypical
- rs2281636CUTC · 99,732,646T;Tcommon in clinvarTypical
- rs717620ABCC2 · 99,782,821C;Ccommon in clinvarTypical
- rs927344ABCC2 · 99,784,690T;Tcommon in complete genomicsTypical
- rs2273697ABCC2 · 99,804,058A;AAdverse reaction more likely to carbamazepine in epileptic patientsMinor
- rs3740071ABCC2 · 99,830,363G;Gcommon genotypeTypical
- rs17222547ABCC2 · 99,831,628C;Ccommon in clinvarTypical
- rs17222723ABCC2 · 99,836,239T;Tcommon on affy axiom dataTypical
- rs3740066ABCC2 · 99,844,450T;T4.4x risk for ICPTypical
- rs8187710ABCC2 · 99,851,537G;Gcommon on affy axiom dataTypical
- rs1119030299,873,158T;TNo summary available.Worth knowing
- rs1324694ERLIN1 · 100,186,688C;Ccommon in complete genomicsTypical
- rs9420790SEC31B · 100,496,440G;Gcommon genotypeTypical
- rs4919510SEMA4G · 100,975,021C;Ccommon in complete genomicsTypical
- rs28937887MRPL43 · 100,989,211G;Gcommon in clinvarTypical
- rs11190870101,219,450T;TPossibly even more increased risk of scoliosisWorth knowing
- rs3758549GBF1 · 102,244,438G;Gincreased risk of parkinson's diseaseMinor
- rs12414407SUFU · 102,627,262T;Tcommon in clinvarTypical
- rs17115100CYP17A1 · 102,831,636T;TIncreased risk of developing Parkinson's DiseaseWorth knowing
- rs1004467CYP17A1 · 102,834,750A;ANo summary available.Typical
- rs6162CYP17A1 · 102,837,224G;Gcommon in clinvarTypical
- rs743572CYP17A1 · 102,837,395A;Acommon in clinvarTypical
- rs2486758CYP17A1 · 102,837,723C;CSlightly higher prostate cancer risk; poorer response to AA/P treatmentWorth knowing
- rs17724534LOC107984264 · 102,845,764C;Ccommon in complete genomicsTypical
- rs11191439BORCS7-ASMT · 102,878,966T;Tcommon on affy axiom dataTypical
- rs12413409CNNM2 · 102,959,339G;GNo summary available.Typical
- rs11191548CNNM2 · 103,086,421T;TNo summary available.Typical
- rs11598702NT5C2 · 103,138,228T;Tcommon in clinvarTypical
- rs11191580NT5C2 · 103,146,454T;Tcommon on affy axiom dataTypical
- rs10883841NT5C2 · 103,174,952T;Tcommon on affy axiom dataTypical
- rs7071247NEURL1 · 103,498,029G;GNo summary available.Typical
- rs7913069LOC102724351 · 103,954,641C;T1.47x risk for uterine fibroidsWorth knowing
- rs17116350COL17A1 · 104,033,992T;Tcommon in clinvarTypical
- rs805722COL17A1 · 104,050,642C;CNo summary available.Typical
- rs805698COL17A1 · 104,057,158C;Ccommon in clinvarTypical
- rs805708COL17A1 · 104,064,575A;ANo summary available.Typical
- rs1320448COL17A1 · 104,086,316G;Gcommon in complete genomicsTypical
- rs4925GSTO1 · 104,263,031C;Ccommon/normalTypical
- rs17119461LOC101927549 · 105,756,594T;Tcommon on affy axiom dataTypical
- rs1359645LOC102724439 · 106,285,899A;Acommon in complete genomicsTypical
- rs3731566ADD3 · 110,126,331A;AnormalTypical
- rs716595MXI1 · 110,246,728G;Gcommon on affy axiom dataTypical
- rs7911129SMC3 · 110,581,113A;Acommon in complete genomicsTypical
- rs1856801110,632,404G;Gcommon in complete genomicsTypical
- rs7082195RBM20 · 110,667,691C;Ccommon in complete genomicsTypical
- rs11195419ADRA2A · 111,079,610C;Ccommon in complete genomicsTypical
- rs553668ADRA2A · 111,079,821G;Gcommon/normalTypical
- rs3814570TCF7L2 · 112,948,751C;T1.3x increased risk for Crohn's disease with ileal involvementMinor
- rs4506565TCF7L2 · 112,996,282T;T1.9x increased risk for type-2 diabetesWorth knowing
- rs7903146TCF7L2 · 112,998,590T;T2x increased risk for Type-2 diabetesImportant
- rs12255372TCF7L2 · 113,049,143T;Tslight increases (~1.5x) in risk for type-2 diabetes and possibly breast cancer and aggressive prostate cancerWorth knowing
- rs7080536HABP2 · 113,588,287A;Asignificant increase (2 - 6x?) in risk possible for carotid stenosis, stroke and venous thromboembolismImportant
- rs12415607CASP7 · 113,678,445C;Ccommon in complete genomicsTypical
- rs10553596CASP7 · 113,679,882TT;TTcommon/normalTypical
- rs11593766CASP7 · 113,697,505T;Tcommon on affy axiom dataTypical
- rs82625113,996,371C;Ccommon in complete genomicsTypical
- rs1801252ADRB1 · 114,044,277G;GNo summary available.Important
- rs1801253ADRB1 · 114,045,297C;Cresponds well to bucindolol; may also depend on rs1801252Minor
- rs17095681SHTN1 · 117,101,266G;Gcommon genotypeTypical
- rs363387SLC18A2 · 117,244,053T;TNo summary available.Typical
- rs363224SLC18A2 · 117,263,062A;AProtective against TD occurrenceMinor
- rs6585436LOC105378502 · 117,450,864T;TNo summary available.Typical
- rs1312895118,667,800C;Ccommon in complete genomicsTypical
- rs1247118118,669,247G;Gcommon in complete genomicsTypical
- rs17098707GRK5 · 119,326,585A;Acommon in complete genomicsTypical
- rs2234962BAG3 · 119,670,121T;Tcommon on affy axiom dataTypical
- rs2252004121,085,195C;Ccommon in complete genomicsTypical
- rs2901286LOC105378522 · 121,141,109C;Ccommon in complete genomicsTypical
- rs10510089LOC105378522 · 121,148,705C;TNo summary available.Typical
- rs17101921121,393,781G;Gcommon in complete genomicsTypical
- rs4752566FGFR2 · 121,508,117G;Tassociated with thicker hair in AsiansMinor
- rs3135753FGFR2 · 121,521,144T;Tcommon genotypeTypical
- rs1047100FGFR2 · 121,538,644T;Tcommon in clinvarTypical
- rs755793FGFR2 · 121,551,357A;Acommon in complete genomicsTypical
- rs2303568FGFR2 · 121,564,448A;Acommon in complete genomicsTypical
- rs3750817FGFR2 · 121,573,063T;T0.64x reduced risk for breast cancer, and higher likelihood of favorable postmenopausal hormone therapyWorth knowing
- rs7895676FGFR2 · 121,574,483C;CnormalTypical
- rs11200014FGFR2 · 121,575,416A;A1.64x risk for breast cancerTypical
- rs2981579FGFR2 · 121,577,821G;GcommonTypical
- rs2981578FGFR2 · 121,580,797T;TnormalTypical
- rs1219648FGFR2 · 121,586,676G;G1.64x risk for breast cancerWorth knowing
- rs2420946FGFR2 · 121,591,810T;T1.64x risk for breast cancerWorth knowing
- rs2981582FGFR2 · 121,592,803A;A1.7x higher risk of ER+ breast cancerImportant
- rs4146894PLEKHA1 · 122,395,865T;T9.1x risk for AMD, but replication is lackingWorth knowing
- rs10490923ARMS2 · 122,454,735G;Gcommon in complete genomicsTypical
- rs2736911LOC105378525 · 122,454,839C;Ccommon in clinvarTypical
- rs10490924LOC105378525 · 122,454,932T;T8.2x risk for age related macular degenerationImportant
- rs17623531ARMS2 · 122,455,405C;Ccommon in complete genomicsTypical
- rs3750847ARMS2 · 122,455,905C;Ccommon in clinvarTypical
- rs2014307LOC105378525 · 122,458,116T;Tincreased risk of age-related macular degenerationTypical
- rs11200638HTRA1 · 122,461,028A;A~10x increased risk of wet age related macular degenerationImportant
- rs1049331HTRA1 · 122,461,754C;Ccommon in clinvarTypical
- rs2284665HTRA1 · 122,467,114G;Gcommon in clinvarTypical
- rs2981745DMBT1 · 122,560,678C;T1.6x increased risk for breast cancer in females over 60Minor
- rs11523871DMBT1 · 122,570,194A;C1.6x increased breast cancer risk for women over 60Minor
- rs7900929124,896,430A;Acommon in complete genomicsTypical
- rs7086128124,898,804A;Acommon in complete genomicsTypical
- rs17152408ZRANB1 · 124,960,438G;Gcommon in complete genomicsTypical
- rs17152411ZRANB1 · 124,960,947A;Acommon in complete genomicsTypical
- rs9422897TEX36 · 125,607,576G;Gcommon in complete genomicsTypical
- rs4385801UROS · 125,823,221G;Gcommon in clinvarTypical
- rs4751440NPS · 127,552,592G;Gcommon on affy axiom dataTypical
- rs11818629128,338,841C;Ccommon on affy axiom dataTypical
- rs568404129,233,875G;Gcommon in complete genomicsTypical
- rs1803965MGMT · 129,707,928C;Ccommon in complete genomicsTypical
- rs12917MGMT · 129,708,019C;Ccommon in complete genomicsTypical
- rs2308321MGMT · 129,766,800A;Acommon in complete genomicsTypical
- rs2308327MGMT · 129,766,906A;AnormalTypical
- rs4751185130,258,151C;Ccommon in complete genomicsTypical
- rs11017328130,548,836C;Ccommon genotypeTypical
- rs10741243TCERG1L · 131,149,699G;Gcommon in complete genomicsTypical
- rs2275725ADAM8 · 133,275,531G;Gcommon on affy axiom dataTypical
- rs3813865CYP2E1 · 133,525,740G;Gcommon in complete genomicsTypical
- rs3813867CYP2E1 · 133,526,101C;CCYP2E1_-1295G>C homozygoteTypical
- rs2031920CYP2E1 · 133,526,341C;CnormalTypical
- rs2070672CYP2E1 · 133,527,044G;GCYP2E1*7_-352A>G homozygoteWorth knowing
- rs2070673CYP2E1 · 133,527,063A;ACYP2E1*7_-333T>A homozygoteTypical
- rs6413420CYP2E1 · 133,527,325G;GnormalTypical
- rs6413419CYP2E1 · 133,532,171A;ACYP2E1*4 homozygoteTypical
- rs915908CYP2E1 · 133,533,455G;Gcommon in complete genomicsTypical
- rs915909CYP2E1 · 133,533,893C;CnormalTypical
- rs4646976CYP2E1 · 133,534,223A;AnormalTypical
- rs6413432CYP2E1 · 133,535,040A;ACYP2E1_marker9 homozygoteTypical
- rs2070676CYP2E1 · 133,537,633G;GCYP2E1*1B homozygoteWorth knowing
- rs2515641CYP2E1 · 133,537,858T;TCYP2E1_10463T>C(F421F) homozygoteWorth knowing
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.