Chromosome 3
390 well-documented SNPs on chromosome 3, in order of position (GRCh38).
- rs6795349LOC107986057 · 130,794A;Acommon in complete genomicsTypical
- rs892295CHL1 · 355,870G;Gcommon genotypeTypical
- rs105102171,798,009G;Gcommon in complete genomicsTypical
- rs2619566CNTN4 · 2,583,254A;ANo summary available.Typical
- rs3804795IL5RA · 3,088,961T;Tcommon in complete genomicsTypical
- rs16727433,190,154A;Acommon genotypeTypical
- rs9835812LOC100130207 · 3,334,100G;Gcommon in complete genomicsTypical
- rs2819590SUMF1 · 4,467,058C;Ccommon in clinvarTypical
- rs2322734ITPR1 · 4,591,808A;Acommon genotypeTypical
- rs17786144ITPR1 · 4,787,891T;Tcommon in complete genomicsTypical
- rs3749380GRM7 · 6,861,610C;Ccommon/normalTypical
- rs11928865GRM7 · 7,114,015T;Tcommon/normalTypical
- rs13317787LOC105376947 · 8,100,265C;Ccommon genotypeTypical
- rs1008642CAV3 · 8,733,975C;Ccommon in clinvarTypical
- rs72546668CAV3 · 8,745,644C;Ccommon in clinvarTypical
- rs1042778OXTR · 8,752,859T;TSlightly lower oxytocin & empathy? Possibly higher 'callous-unemotional' trait frequency in children.Minor
- rs237885OXTR · 8,753,857G;Tcommon in complete genomicsTypical
- rs2268494OXTR · 8,760,360T;TNo summary available.Typical
- rs13316193OXTR · 8,761,057C;Cslight evidence indicating increased OXTR expression, higher levels of empathy.Typical
- rs53576OXTR · 8,762,685A;ALack of empathy?Worth knowing
- rs1052133OGG1 · 9,757,089G;G2x increased bladder cancer risk; 4.5x increased risk for gallbladder cancerWorth knowing
- rs279552CRELD1 · 9,934,475A;Acommon in clinvarTypical
- rs779805VHL · 10,141,653G;Gcommon in clinvarTypical
- rs104893829VHL · 10,142,088C;Ccommon in clinvarTypical
- rs587780077VHL · 10,146,618A;GVon Hippel-Lindau syndrome mutationVery important
- rs5030814VHL · 10,146,638G;TVon Hippel-Lindau syndrome mutationVery important
- rs1678607VHL · 10,146,744G;Gcommon/normalTypical
- rs5030818VHL · 10,149,804C;TVon Hippel-Lindau syndrome mutationVery important
- rs28940298VHL · 10,149,921C;Ccommon in clinvarTypical
- rs1642742VHL · 10,150,259G;Gcommon in clinvarTypical
- rs11465886IRAK2 · 10,209,099A;Acommon genotypeTypical
- rs4684677GHRL · 10,286,769T;Tcommon on affy axiom dataTypical
- rs696217GHRL · 10,289,773G;Gcommon in clinvarTypical
- rs2675163SLC6A1 · 11,033,328T;Tcommon in complete genomicsTypical
- rs7651620HRH1 · 11,259,846G;Gcommon in complete genomicsTypical
- rs6777876SETP19 · 11,915,124A;Acommon on affy axiom dataTypical
- rs1703610112,236,345G;Gcommon on affy axiom dataTypical
- rs1308138912,248,301A;Acommon on affy axiom dataTypical
- rs17036170PPARG · 12,288,912A;AElevated risk for drug induced liver injury with diclofenacWorth knowing
- rs17036314PPARG · 12,335,246C;Crisk of progressing from IGT to T2D; reduced by exerciseTypical
- rs6802898PPARG · 12,349,708C;CNo summary available.Typical
- rs2197423PPARG · 12,350,084G;GNo summary available.Typical
- rs17241090PPARG · 12,351,626C;CNo summary available.Typical
- rs1801282PPARG · 12,351,626C;GUnconfirmed higher risk of cardiovascular disease with high saturated fat dietImportant
- rs1899951PPARG · 12,353,341C;CNo summary available.Typical
- rs13306747PPARG · 12,416,775C;Ccommon in clinvarTypical
- rs3856806PPARG · 12,434,058C;Ccommon in clinvarTypical
- rs3729931RAF1 · 12,585,017G;Gcommon in clinvarTypical
- rs3730271RAF1 · 12,604,195A;TNoonan syndromeVery important
- rs9846232LINC00620 · 13,701,633G;Gcommon in complete genomicsTypical
- rs113449357TMEM43 · 14,139,231C;Tlikely to be benignTypical
- rs63750743TMEM43 · 14,141,665C;TArrhythmogenic right ventricular dysplasiaVery important
- rs1043953TMEM43 · 14,142,258A;Acommon in clinvarTypical
- rs2228001XPC · 14,145,949T;TNo summary available.Typical
- rs2279017LOC107986063 · 14,148,737T;Tcommon in clinvarTypical
- rs2470353LOC107986063 · 14,148,768G;Gcommon in clinvarTypical
- rs1124303XPC · 14,154,182T;TNo summary available.Typical
- rs2228000XPC · 14,158,387A;Astatistically significant, but slight, increase in bladder cancer riskMinor
- rs1870134XPC · 14,178,523G;Gcommon in clinvarTypical
- rs3731055LSM3 · 14,178,939C;Ccommon in complete genomicsTypical
- rs869025342CCDC174 · 14,671,194G;GInfantile hypotonia with psychomotor retardationVery important
- rs7639618DVWA · 15,174,922C;T1.45x increased osteoarthritis riskWorth knowing
- rs11718863DVWA · 15,175,196A;AnormalTypical
- rs9864422COL6A4P1 · 15,185,745C;CnormalTypical
- rs13073139BTD · 15,644,367G;Gcommon in clinvarTypical
- rs13078881BTD · 15,645,186C;CBiotinidase deficiency; note ability to treat & variable penetranceVery important
- rs10510468PLCL2 · 16,897,125G;Gcommon in complete genomicsTypical
- rs6767049SGO1-AS1 · 20,179,220G;Tcommon in complete genomicsTypical
- rs199815268SGO1-AS1 · 20,183,961C;CCAID (chronic atrial and intestinal dysrhythmia) predictedVery important
- rs3821396ZNF385D · 21,664,877G;Gcommon on affy axiom dataTypical
- rs9816269ZNF385D · 21,677,349T;Tcommon genotypeTypical
- rs11719664ZNF385D · 21,913,706C;Ccommon on affy axiom dataTypical
- rs12630816RARB · 25,426,257C;CNo summary available.Typical
- rs17016462RARB · 25,474,625A;Acommon in complete genomicsTypical
- rs1435703RARB · 25,518,740G;Gcommon in complete genomicsTypical
- rs201337954NGLY1 · 25,733,931A;AHomozygous for defective NGLY1 allele, leading to congenital disorder of deglycosylation (CDDG)Very important
- rs669607LOC107986041 · 28,029,953A;Ccommon in complete genomicsTypical
- rs17093428,037,594C;Tcommon in complete genomicsTypical
- rs4399848LINC00693 · 28,662,972A;ArareTypical
- rs1530057RBMS3 · 29,533,972G;Gcommon in complete genomicsTypical
- rs1051063430,305,477A;Acommon in complete genomicsTypical
- rs2228048TGFBR2 · 30,672,350C;Ccommon in complete genomicsTypical
- rs11466532TGFBR2 · 30,692,953C;Ccommon in clinvarTypical
- rs17026688GADL1 · 30,845,325C;TNo summary available.Worth knowing
- rs17027625THRAP3P1 · 31,404,088T;Tcommon in complete genomicsTypical
- rs4276227CMTM8 · 32,289,194C;C1.5x riskTypical
- rs12638540CMTM7 · 32,447,042A;Acommon in complete genomicsTypical
- rs984547532,800,609T;Tcommon on affy axiom dataTypical
- rs4302331GLB1 · 33,014,229A;Acommon in clinvarTypical
- rs677025734,143,013T;TNo summary available.Typical
- rs1703350635,598,334G;Gcommon genotypeTypical
- rs679970535,940,638C;Ccommon in complete genomicsTypical
- rs1800734MLH1 · 36,993,455G;Gcommon in clinvarTypical
- rs11541859MLH1 · 37,001,012G;TLynch syndrome, pathogenic mutationVery important
- rs1540354MLH1 · 37,002,998A;Acommon in clinvarTypical
- rs1799977MLH1 · 37,012,077A;Acommon in clinvarTypical
- rs63750198MLH1 · 37,014,509A;Apossible Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2)Very important
- rs4647269MLH1 · 37,016,100C;Ccommon in clinvarTypical
- rs63750710MLH1 · 37,020,411A;CLynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2)Very important
- rs10849LRRFIP2 · 37,053,579C;Ccommon in clinvarTypical
- rs9311171CTDSPL · 37,954,986T;Tcommon in complete genomicsTypical
- rs1805126SCN5A · 38,550,915A;Acommon in clinvarTypical
- rs137854604SCN5A · 38,551,243A;Gpossibility of idiopathic ventricular fibrillationImportant
- rs41261344SCN5A · 38,575,385C;TProbably benign; previously, thought to confer possible susceptibility to long QT syndromeMinor
- rs7626962SCN5A · 38,579,416G;TNow: Benign? Formerly: increased susceptibility to long QT syndromeWorth knowing
- rs11708996SCN5A · 38,592,432G;Gcommon on affy axiom dataTypical
- rs36210423SCN5A · 38,603,887T;Tlikely to be benignTypical
- rs1805124SCN5A · 38,603,929T;Tcommon in clinvarTypical
- rs3918389SCN5A · 38,603,948C;Ccommon in clinvarTypical
- rs28937318SCN5A · 38,606,709T;TBrugada syndrome 1Very important
- rs45471994SCN5A · 38,613,752C;Ccommon in clinvarTypical
- rs45546039SCN5A · 38,613,781T;Tassociated with cardiomyopathy and arrhythmiasVery important
- rs45620037SCN5A · 38,613,787A;GNow: Probably benign. Formerly: increased risk for dilated cardiomyopathyMinor
- rs11710077SCN5A · 38,616,408A;Acommon in complete genomicsTypical
- rs6791924SCN5A · 38,633,208G;Gcommon in complete genomicsTypical
- rs6771157SCN10A · 38,722,372G;Gcommon in clinvarTypical
- rs12632942SCN10A · 38,723,507A;Acommon in clinvarTypical
- rs6795970SCN10A · 38,725,184A;Acommon in clinvarTypical
- rs3732378CX3CR1 · 39,265,671A;Amore rapid progression to full-blown AIDS and probably increased susceptibility to HIV infectionWorth knowing
- rs3732379CX3CR1 · 39,265,765C;CnormalTypical
- rs1703882839,433,851C;Ccommon genotypeTypical
- rs538867MOBP · 39,471,787C;Ccommon genotypeTypical
- rs816488MOBP · 39,512,297T;Tcommon in complete genomicsTypical
- rs1707953439,805,581A;AIncreased odds of relapse in treated childhood ALL patientsWorth knowing
- rs9985399MYRIP · 39,967,143T;Tcommon in complete genomicsTypical
- rs1052501ULK4 · 41,883,906C;Ccommon in clinvarTypical
- rs2272007ULK4 · 41,954,644T;Tcommon in clinvarTypical
- rs754635CCK · 42,263,639G;Gcommon in complete genomicsTypical
- rs1799923CCK · 42,264,802G;Gcommon in complete genomicsTypical
- rs2286720LYZL4 · 42,406,979G;Gcommon on affy axiom dataTypical
- rs2228467ACKR2 · 42,864,624T;TNo summary available.Typical
- rs1707528643,189,231C;Ccommon in complete genomicsTypical
- rs17279437SLC6A20 · 45,772,602G;Gcommon on affy axiom dataTypical
- rs758386SLC6A20 · 45,775,926G;GNo summary available.Typical
- rs7652331FYCO1 · 45,921,260C;Cnormal riskTypical
- rs1545985FYCO1 · 45,963,986A;Anormal riskTypical
- rs17282391LOC105377067 · 46,137,989A;Acommon in complete genomicsTypical
- rs13084057LOC105377067 · 46,143,233C;Ccommon in complete genomicsTypical
- rs7616215LOC105377067 · 46,164,194T;TNormalTypical
- rs1309891146,193,709C;Ccommon in complete genomicsTypical
- rs13075270CCR3 · 46,212,298T;Tcommon in complete genomicsTypical
- rs13092160CCR3 · 46,213,300T;Tcommon in complete genomicsTypical
- rs1171105446,304,120A;Acommon/normalTypical
- rs6441961LOC100131327 · 46,310,893C;Ccommon/normalTypical
- rs1799864CCR2 · 46,357,717A;ANo summary available.Typical
- rs2856758CCR5 · 46,370,170A;Acommon in complete genomicsTypical
- rs333CCR5 · 46,373,456-;-very resistant to HIVVery important
- rs6808835CCRL2 · 46,408,373G;Gcommon in complete genomicsTypical
- i3003626CCR5 · 46,414,947D;Dresistant to HIVVery important
- rs6791599LOC105377068 · 46,417,451G;Gcommon in complete genomicsTypical
- rs9110LTF · 46,439,310A;Acommon in complete genomicsTypical
- rs7626978ATRIP · 48,464,432T;Tcommon in complete genomicsTypical
- rs3135941TREX1 · 48,466,268T;Tcommon in clinvarTypical
- rs2228563COL7A1 · 48,586,607C;Ccommon in complete genomicsTypical
- rs2228561COL7A1 · 48,590,581G;Gcommon on affy axiom dataTypical
- rs35713889LAMB2 · 49,125,150C;Ccommon in clinvarTypical
- rs1050450GPX1 · 49,357,401A;GIncreased risk of damage caused by oxidative stress in many diseasesMinor
- rs8179164RHOA · 49,359,851T;Tcommon in complete genomicsTypical
- rs9858542BSN · 49,664,550A;A1.8x risk of Crohn's diseaseMinor
- rs3197999MST1 · 49,684,099A;A1.2x risk of Crohn'sWorth knowing
- rs1128535TRAIP · 49,828,959C;Creduced risk (0.77x) for Crohn's diseaseWorth knowing
- rs2072054SEMA3F · 50,159,190A;Acommon in complete genomicsTypical
- rs2071203SEMA3B · 50,274,469C;Ccommon in complete genomicsTypical
- rs11130248HYAL1 · 50,314,769A;Acommon in complete genomicsTypical
- rs781999115HYAL2 · 50,319,741A;ACleft lip and palate; possible heart abnormalitiesVery important
- rs2239751CISH · 50,610,457T;Tcommon in complete genomicsTypical
- rs3792323MAPKAPK3 · 50,622,900A;Acommon in complete genomicsTypical
- rs13088462DOCK3 · 51,034,282T;TNo summary available.Typical
- rs387906848BAP1 · 52,402,608A;GBAP1 Tumor Predisposition SyndromeVery important
- rs6784615NISCH · 52,472,410T;Tcommon on affy axiom dataTypical
- rs2251219PBRM1 · 52,550,771C;TLower bipolar disorder risk?Typical
- rs6976GLT8D1 · 52,694,788C;CNo increased risk of osteoarthritisMinor
- rs2564921RFT1 · 53,091,569T;Tcommon in clinvarTypical
- rs312481CACNA1D · 53,517,875G;Gbetter response to certain calcium channel blockersTypical
- rs3774426CACNA1D · 53,524,975C;Cbetter response to certain calcium channel blockersTypical
- rs1401492CACNA1D · 53,646,097C;Ccommon in complete genomicsTypical
- rs13074914CACNA2D3 · 54,496,558G;Gcommon in complete genomicsTypical
- rs35880655,279,372C;C1.78x increased risk of developing Type-2 diabetesWorth knowing
- rs1875110ERC2 · 55,529,316T;Tcommon genotypeTypical
- rs7646054ARHGEF3 · 56,775,600A;AnormalTypical
- rs9834312FLNB · 58,096,982A;AnormalTypical
- rs6445975PXK · 58,384,450G;GSystemic lupus erythematosus disease risk associated in EuropeansWorth knowing
- rs13315591LOC107984079 · 58,571,114T;TNo summary available.Typical
- rs4502542FHIT · 59,935,294C;Ccommon genotypeTypical
- rs10510837FHIT · 60,304,113G;Gcommon on affy axiom dataTypical
- rs6791644FHIT · 60,785,375A;ANo summary available.Typical
- rs10514718LOC105377114 · 61,428,140C;Ccommon on affy axiom dataTypical
- rs10490775PTPRG · 62,051,050C;Ccommon on affy axiom dataTypical
- rs304172CADPS · 62,796,793G;Gcommon genotypeTypical
- rs3774729ATXN7 · 63,996,406G;Gcommon in clinvarTypical
- rs6795735ADAMTS9-AS2 · 64,719,689C;Ccommon in clinvarTypical
- rs9827908LRIG1 · 66,395,177A;Acommon genotypeTypical
- rs13078828LRIG1 · 66,429,063G;Gcommon genotypeTypical
- rs17045031LOC105377142 · 66,717,940G;Gcommon in complete genomicsTypical
- rs1306904966,759,518A;Acommon in complete genomicsTypical
- rs1170962566,772,733C;CNo summary available.Typical
- rs17047573FAM19A1 · 68,361,969T;Tcommon in complete genomicsTypical
- rs17047586FAM19A1 · 68,363,724A;Acommon in complete genomicsTypical
- rs6806528FRMD4B · 69,203,748C;Ccommon on affy axiom dataTypical
- rs13063872FOXP1 · 71,415,184G;GNo summary available.Typical
- rs12629971EIF4E3 · 71,734,167C;Ccommon in complete genomicsTypical
- rs6801173EIF4E3 · 71,746,592C;Ccommon in complete genomicsTypical
- rs11128271LOC105377160 · 72,460,120C;Ccommon genotypeTypical
- rs983231472,468,889A;Acommon genotypeTypical
- rs9824246PPP4R2 · 73,053,574A;Acommon in complete genomicsTypical
- rs10511052ROBO2 · 76,676,752G;Gcommon genotypeTypical
- rs2172397GBE1 · 81,594,016C;Ccommon in complete genomicsTypical
- rs2229519GBE1 · 81,648,979T;Tcommon in clinvarTypical
- rs1051108984,431,917G;Gcommon on affy axiom dataTypical
- rs13078807CADM2 · 85,835,000A;Acommon, despite what hapmap saysTypical
- rs17023661LOC105377196 · 86,919,359C;Ccommon genotypeTypical
- rs138925964PROS1 · 93,879,279T;TClotting issues likely in infantsVery important
- rs121918472PROS1 · 93,879,306G;GIncreased venous thromboembolism risk (> 6x)Very important
- rs5017717PROS1 · 93,884,869G;Gcommon in clinvarTypical
- rs679602696,609,983C;Ccommon genotypeTypical
- rs832081MINA · 97,961,230G;Gcommon in complete genomicsTypical
- rs1497546LOC105373999 · 98,315,682G;Gcommon in complete genomicsTypical
- rs13070584LOC105374005 · 99,547,493C;Ccommon in complete genomicsTypical
- rs13095226COL8A1 · 99,677,428T;Tcommon in complete genomicsTypical
- rs13081855COL8A1 · 99,762,695G;Gcommon in clinvarTypical
- rs2063640102,484,201C;Ccommon on affy axiom dataTypical
- rs6806362LOC100287880 · 103,172,459G;Gcommon in complete genomicsTypical
- rs6437585ALCAM · 105,367,241C;Ccommon in complete genomicsTypical
- rs11559013ALCAM · 105,575,658G;Gcommon in complete genomicsTypical
- rs3772534CBLB · 105,702,190G;GNo summary available.Typical
- rs12487066LOC105374027 · 106,193,283C;C>1.09x increased risk for multiple sclerosisTypical
- rs3900940MYH15 · 108,428,881C;Cslightly increased risk of coronary heart diseaseTypical
- rs769554LINC01205 · 109,485,566G;GNo summary available.Typical
- rs4450776PLCXD2 · 111,704,282C;Ccommon on affy axiom dataTypical
- rs9288952BTLA · 112,466,178A;Acommon in complete genomicsTypical
- rs2931761BTLA · 112,471,290T;Tcommon in complete genomicsTypical
- rs2633562BTLA · 112,477,584T;Tcommon in complete genomicsTypical
- rs2705535BTLA · 112,490,080C;Ccommon in complete genomicsTypical
- rs9811423113,103,475C;Gcommon in complete genomicsTypical
- rs7611694SIDT1 · 113,556,777C;CLower prostate cancer risk?Minor
- rs2251177DRD3 · 114,139,503C;Ccommon in clinvarTypical
- rs2630349DRD3 · 114,154,525G;Gcommon in complete genomicsTypical
- rs2630351DRD3 · 114,156,212G;Gcommon in complete genomicsTypical
- rs167771DRD3 · 114,157,428G;GNo summary available.Minor
- rs324032DRD3 · 114,158,981A;Acommon in complete genomicsTypical
- rs3732783DRD3 · 114,171,942T;Tcommon in clinvarTypical
- rs6280DRD3 · 114,171,968C;Cbetter response to olanzapineTypical
- rs16829840TMEM39A · 119,429,111C;Ccommon genotypeTypical
- rs1132200TMEM39A · 119,431,989C;Ccommon on affy axiom dataTypical
- rs12721613NR1I2 · 119,807,329C;Ccommon in complete genomicsTypical
- rs12721607NR1I2 · 119,807,356G;Gcommon in complete genomicsTypical
- rs6438552GSK3B · 119,912,967A;GNo summary available.Typical
- rs11919783GSK3B · 120,027,786G;GNo summary available.Typical
- rs334558LOC107986119 · 120,094,435A;Alater onset of BPTypical
- rs2255543HGD · 120,670,469T;Tcommon in clinvarTypical
- rs6800901POLQ · 121,435,346T;T1.3x multiple myeloma riskMinor
- rs1141528IQCB1 · 121,788,384A;Acommon in clinvarTypical
- rs9282641CD86 · 122,077,921G;Gcommon in complete genomicsTypical
- rs17251221CASR · 122,274,400A;Acommon on affy axiom dataTypical
- rs1801725CASR · 122,284,910G;Gcommon in clinvarTypical
- rs1042636CASR · 122,284,922A;Acommon in complete genomicsTypical
- rs1801726CASR · 122,284,985G;Gcommon in clinvarTypical
- rs9740CASR · 122,286,206A;Acommon in clinvarTypical
- rs17265703CSTA · 122,329,797A;Acommon on affy axiom dataTypical
- rs2173763PARP15 · 122,610,313A;Acommon in complete genomicsTypical
- rs796065306ADCY5 · 123,319,754C;TDyskinesia, familial, with facial myokymiaVery important
- rs1234FAKE1 · 123,615,654A;Asummary of something badWorth knowing
- rs40305MYLK · 123,692,742G;Gcommon in clinvarTypical
- rs2222823MYLK · 123,885,940T;Tcommon in complete genomicsTypical
- rs9289231KALRN · 124,055,231T;TNo summary available.Typical
- rs6438833KALRN · 124,206,748T;Tcommon in complete genomicsTypical
- rs1801019UMPS · 124,737,895G;Gcommon in clinvarTypical
- rs1055419OSBPL11 · 125,594,988G;Gcommon in complete genomicsTypical
- rs3803GATA2 · 128,480,537G;Gcommon in clinvarTypical
- rs2713604GATA2 · 128,481,616A;GNo summary available.Typical
- rs2335052GATA2 · 128,486,108C;Ccommon in clinvarTypical
- rs140693MBD4 · 129,436,608C;Ccommon in complete genomicsTypical
- rs2269736RHO · 129,528,683G;Gcommon in complete genomicsTypical
- rs7984RHO · 129,528,708A;Acommon in clinvarTypical
- rs387907571DNAJC13 · 132,477,995A;GParkinson's disease, possibleVery important
- rs2369955132,974,744A;Acommon on affy axiom dataTypical
- rs1130459TF · 133,746,439A;Acommon in clinvarTypical
- rs1799852TF · 133,756,878T;Tlower serum transferrin levelsWorth knowing
- rs1799899TF · 133,756,968G;Gcommon in complete genomicsTypical
- rs2692696TF · 133,766,289G;Gcommon in complete genomicsTypical
- rs1049296TF · 133,775,510T;TC2 transferrin subtype; very slightly higher risk for AlzheimersMinor
- rs9844666PCCB · 136,255,374A;GAMD associationTypical
- rs9826828STAG1 · 136,683,218G;Gcommon genotypeTypical
- rs2306374MRAS · 138,401,110C;CIncreased risk for CHDTypical
- rs1511412138,994,862G;Gcommon on affy axiom dataTypical
- rs1873668139,326,219G;Gcommon in complete genomicsTypical
- rs4243399139,332,068A;Acommon in complete genomicsTypical
- rs16849083RBP2 · 139,465,437C;Ccommon in complete genomicsTypical
- rs6439886CLSTN2 · 139,963,653A;Anormal formTypical
- rs17411949CLSTN2 · 140,380,851C;CNo summary available.Typical
- rs17348572LOC105374132 · 140,459,539T;Tcommon in complete genomicsTypical
- rs4683505CLSTN2 · 140,528,335C;Ccommon genotypeTypical
- rs9850224140,856,445G;Gcommon genotypeTypical
- rs16851254PXYLP1 · 141,260,569A;Acommon genotypeTypical
- rs6763931ZBTB38 · 141,383,991A;ANo summary available.Typical
- rs9825379ZBTB38 · 141,418,193G;Gcommon in complete genomicsTypical
- rs10513137ZBTB38 · 141,424,588G;Gcommon in complete genomicsTypical
- rs11921014141,657,298C;Ccommon genotypeTypical
- rs2227928ATR · 142,562,770G;Gpoorer response to pancreatic cancer combined treatmentTypical
- rs3773506PLS1 · 142,712,158G;Gcommon on affy axiom dataTypical
- rs17636071SLC9A9 · 143,286,187T;TNo summary available.Typical
- rs4839680144,183,185T;TNo summary available.Typical
- rs345013145,456,001A;Acommon on affy axiom dataTypical
- rs12629805146,914,377C;CNo summary available.Typical
- rs1492099AGTR1 · 148,719,716C;CNo summary available.Typical
- rs5182AGTR1 · 148,741,608C;Ccommon in clinvarTypical
- rs5186AGTR1 · 148,742,201C;C7.3x increased risk of hypertensionImportant
- rs267606858GYG1 · 148,996,406T;TLikely miscall in DNA-chip based data, such as that from Ancestry or 23andMe; otherwise, Glycogen storage disease XVVery important
- rs701753CP · 149,198,448A;Acommon in complete genomicsTypical
- rs6809699P2RY12 · 151,338,810A;Acommon in clinvarTypical
- rs6785930P2RY12 · 151,338,828G;Gcommon in clinvarTypical
- rs10513432ATP5LP5 · 152,817,576T;Tcommon genotypeTypical
- rs701265P2RY1 · 152,836,568A;Acommon in complete genomicsTypical
- rs6778194LOC105374165 · 153,466,867A;ANo summary available.Typical
- rs573872LOC105374165 · 153,754,374T;Tcommon in complete genomicsTypical
- rs2665390TIPARP · 156,679,960C;C1.4x increased risk for ovarian cancerMinor
- rs7651446TIPARP · 156,689,208T;T2.25x increased risk for epithelial ovarian cancerWorth knowing
- rs13064954157,136,953G;Gcommon in complete genomicsTypical
- rs9866141TRNAI28P · 157,232,790C;Ccommon in complete genomicsTypical
- rs17810546IL12A-AS1 · 159,947,262A;Acommon in complete genomicsTypical
- rs2243115IL12A · 159,988,493T;Tcommon in complete genomicsTypical
- rs6441286IL12A-AS1 · 160,011,091G;G3.08x chance of developing primary biliary cirrhosisWorth knowing
- rs4855271SI · 164,996,744C;Ccommon in clinvarTypical
- rs1803274BCHE · 165,773,492T;Tpossible increased Alzheimer's riskTypical
- rs1799807BCHE · 165,830,741C;CHomozygous for "atypical" BuChE; see warning re drug (incl. anesthetic) useVery important
- rs12489747166,714,379G;Gcommon in complete genomicsTypical
- rs12696304TERC · 169,763,483C;GProne to aging faster, at least in European populations?Worth knowing
- rs10936599MYNN · 169,774,313C;Clonger telomeres, longer life?Worth knowing
- rs2276717LOC101928583 · 170,483,441C;Ccommon in clinvarTypical
- rs5400SLC2A2 · 171,014,511A;Asignificantly higher sugar consumptionMinor
- rs11920719TNIK · 171,116,770A;Acommon in complete genomicsTypical
- rs6794092171,840,554G;Gcommon on affy axiom dataTypical
- rs2948694GHSR · 172,447,373G;Gincreased risk for heavy alcohol consumptionWorth knowing
- rs572169GHSR · 172,447,937C;Ccommon in clinvarTypical
- rs495225GHSR · 172,448,243G;Gcommon in clinvarTypical
- rs2232165GHSR · 172,448,354G;GnormalTypical
- rs1131532TNFSF10 · 172,506,513G;GnormalTypical
- rs78943174NAALADL2 · 175,534,948C;Ccommon genotypeTypical
- rs6772209175,929,377G;Gcommon in complete genomicsTypical
- rs644695LOC100505566 · 177,573,909A;Acommon on affy axiom dataTypical
- rs7634528LOC105374234 · 178,048,676T;TNo summary available.Typical
- rs9883878178,137,844G;Gcommon genotypeTypical
- rs9290663KCNMB2-AS1 · 178,712,151A;Acommon/normalTypical
- rs4855094PIK3CA · 179,160,189G;Gcommon in complete genomicsTypical
- rs16832889182,133,496A;Acommon genotypeTypical
- rs2270968MCCC1 · 183,037,421T;Tcommon in clinvarTypical
- rs10513789MCCC1 · 183,042,285G;G0.64x decreased risk of Parkinson's diseaseMinor
- rs683395LAMP3 · 183,152,030T;TNo summary available.Typical
- rs514636LAMP3 · 183,152,648A;Acommon in complete genomicsTypical
- rs6807362HTR3C · 184,060,222C;Cincreased autism riskWorth knowing
- rs2971410EIF2B5 · 184,137,983G;Gcommon in clinvarTypical
- rs6141THPO · 184,372,478C;Ccommon in clinvarTypical
- rs4402960IGF2BP2 · 185,793,899T;T1.2x increased risk for type-2 diabetes, 1.5x risk for gestational diabetesWorth knowing
- rs1470579IGF2BP2 · 185,811,292A;AnormalTypical
- rs2002675185,911,780A;Gcommon in complete genomicsTypical
- rs7647305186,116,501C;CObesity riskTypical
- rs2077119AHSG · 186,612,673G;G0.91x decreased risk for T2DTypical
- rs2593813AHSG · 186,614,782C;TNo summary available.Typical
- rs4917AHSG · 186,619,924C;TNo summary available.Typical
- rs10937273186,831,906A;AIn Type 2 diabetics, possibly earlier onset of diseaseMinor
- rs822387186,838,248C;Cmay have higher adiponectin levelsMinor
- rs16861194ADIPOQ · 186,841,636A;Acommon in complete genomicsTypical
- rs17300539ADIPOQ · 186,841,671A;Ahigher adiponectin levelsMinor
- rs266729ADIPOQ · 186,841,685G;G0.73x decreased risk for colorectal cancerWorth knowing
- rs16861205ADIPOQ · 186,843,845G;Gcommon in complete genomicsTypical
- rs17366568ADIPOQ · 186,852,664G;Gcommon in complete genomicsTypical
- rs17366653ADIPOQ · 186,853,027T;Tcommon in complete genomicsTypical
- rs2241766ADIPOQ · 186,853,103G;GSlightly lower risk of breast cancerWorth knowing
- rs1501299ADIPOQ · 186,853,334T;Tslightly lower risk of breast cancerWorth knowing
- rs17366743ADIPOQ · 186,854,300T;TNo summary available.Typical
- rs6444175186,861,955A;AHighest adiponectin levels, presumably much lower obesityTypical
- rs17373414186,867,738C;CNo summary available.Typical
- rs10937275ST6GAL1 · 186,933,001G;GNo summary available.Typical
- rs710466MASP1 · 187,260,154A;Acommon in complete genomicsTypical
- rs6764050187,696,203A;Acommon genotypeTypical
- rs9851967LPP · 188,369,840C;CnormalTypical
- rs4686484LPP · 188,400,784A;Aslightly increased risk for celiac diseaseMinor
- rs1152846LPP · 188,703,109C;Tcommon in complete genomicsTypical
- rs6789327189,395,472G;Gcommon genotypeTypical
- rs7610017TP63 · 189,625,635G;Gcommon in complete genomicsTypical
- rs17505102TP63 · 189,683,987G;Gcommon in complete genomicsTypical
- rs710521189,928,144T;T1.4x increased risk of developing bladder cancer.Worth knowing
- rs16865258LOC107986170 · 190,279,607C;Ccommon in complete genomicsTypical
- rs9869263LOC107986170 · 190,312,891A;Acommon in clinvarTypical
- rs17429833CLDN1 · 190,322,219C;Ccommon in clinvarTypical
- rs12053868IL1RAP · 190,582,215A;Gpossibly faster amyloid accumulation in older (70+) adultsWorth knowing
- rs7635839TRIM16L · 191,949,988G;Gcommon in complete genomicsTypical
- rs9836672FGF12 · 192,195,081C;CNo summary available.Typical
- rs7624750OPA1 · 193,617,202G;Gcommon in clinvarTypical
- rs789852TMEM44 · 194,606,369C;Ccommon in complete genomicsTypical
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.