Chromosome 22
146 well-documented SNPs on chromosome 22, in order of position (GRCh38).
- rs4819554IL17RA · 17,084,145A;Acommon in complete genomicsTypical
- rs2229151IL17RA · 17,108,407G;Gcommon in complete genomicsTypical
- rs882643IL17RA · 17,110,933C;Ccommon in clinvarTypical
- rs8190315BID · 17,743,998T;Tcommon in complete genomicsTypical
- rs450046PRODH · 18,913,491C;Ccommon in clinvarTypical
- rs4819756PRODH · 18,925,165A;GNo summary available.Typical
- rs3747052TSSK2 · 19,131,479A;Acommon in complete genomicsTypical
- rs2073738CLTCL1 · 19,183,443C;Ccommon in complete genomicsTypical
- rs1061325CLTCL1 · 19,196,584C;CTwo copies of "farmer" CLTCL1 gene variantWorth knowing
- rs5748469TXNRD2 · 19,919,576C;Ccommon in clinvarTypical
- rs737865COMT · 19,942,598C;TNo summary available.Typical
- rs4633COMT · 19,962,712C;Thigher risk for endometrial cancerWorth knowing
- rs6267COMT · 19,962,740G;GcommonTypical
- rs740602COMT · 19,962,745G;Gcommon in complete genomicsTypical
- rs8192488COMT · 19,963,714C;Ccommon in complete genomicsTypical
- rs165688COMT · 19,963,748G;GNo summary available.Typical
- rs4680COMT · 19,963,748A;A(worrier) advantage in memory and attention tasksWorth knowing
- rs769224COMT · 19,964,281G;GNo summary available.Typical
- rs165631COMT · 19,964,293C;TPerhaps slightly lower risk for breast cancer in BRCA1/2 mutation carriers?Minor
- rs9332377COMT · 19,968,169C;Ccommon/normalTypical
- rs5993891ARVCF · 19,972,223C;Ccommon in complete genomicsTypical
- rs2239395ARVCF · 19,974,680T;Tcommon in complete genomicsTypical
- rs417309DGCR8 · 20,111,021G;GNo summary available.Typical
- rs175174ZDHHC8 · 20,140,031A;GNo summary available.Typical
- rs5763911KLHL22 · 20,443,002T;Tcommon genotypeTypical
- rs5907SERPIND1 · 20,779,935G;Gcommon in clinvarTypical
- rs1320VPREB1 · 22,245,125G;Gcommon on affy axiom dataTypical
- rs3761418RSPH14 · 23,178,907A;A1.3x increased risk for depressionTypical
- rs2267012BCR · 23,193,795A;A1.3x increased risk for depressionTypical
- rs2267013BCR · 23,203,692G;G1.3x increased risk for depressionMinor
- rs2267015BCR · 23,216,374A;A1.3x increased risk for depressionTypical
- rs2156921BCR · 23,226,876A;G1.29x increased risk for depressionWorth knowing
- rs140504BCR · 23,285,182A;A1.4x increased risk for bipolar disorderTypical
- rs131690BCR · 23,305,822A;Anormal riskTypical
- rs131702BCR · 23,308,800G;GNo summary available.Typical
- rs738792MMP11 · 23,779,191T;Tcommon in complete genomicsTypical
- rs2298383SPECC1L-ADORA2A · 24,429,543C;Cincreased anxiety in response to caffeineWorth knowing
- rs5751876SPECC1L-ADORA2A · 24,441,333T;Tsignificantly higher anxiety levels after moderate caffeine consumptionWorth knowing
- rs4822492ADORA2A-AS1 · 24,447,626C;Cincreased anxiety in response to caffeineWorth knowing
- rs17651189ADORA2A-AS1 · 24,448,915T;Tcommon genotypeTypical
- rs133885MYO18B · 25,763,322A;GNo summary available.Typical
- rs3859866MYO18B · 25,770,933C;Ccommon in complete genomicsTypical
- rs5761170MYO18B · 25,777,694C;Ccommon in complete genomicsTypical
- rs1001021MYO18B · 26,007,633G;Gcommon in complete genomicsTypical
- rs688034SEZ6L · 26,293,669T;T1.6x riskWorth knowing
- rs663048SEZ6L · 26,299,111T;T3x increased risk of developing lung cancerWorth knowing
- rs2014410HPS4 · 26,464,303G;Gcommon in clinvarTypical
- rs713998HPS4 · 26,466,246T;Tcommon in clinvarTypical
- rs744016ISCA2P1 · 26,646,142C;Ccommon in complete genomicsTypical
- rs2331291MIAT · 26,662,857C;TNo summary available.Typical
- rs576231127,694,209G;Gcommon in complete genomicsTypical
- rs555607708CHEK2 · 28,695,869-;Gincreased risk of breast and prostate cancerImportant
- rs28909980CHEK2 · 28,696,957C;Ccommon in clinvarTypical
- rs17879961CHEK2 · 28,725,099T;TNo summary available.Typical
- rs1805129CHEK2 · 28,734,470T;Tcommon in complete genomicsTypical
- rs132390EMID1 · 29,225,488T;Tcommon genotypeTypical
- rs2857461EWSR1 · 29,272,015T;Tcommon in complete genomicsTypical
- rs5763662MTMR3 · 29,982,714C;Ccommon genotypeTypical
- rs2412980LOC105372988 · 30,196,080C;Ccommon on affy axiom dataTypical
- rs42929GAL3ST1 · 30,560,432C;CNo summary available.Typical
- rs9606756TCN2 · 30,610,873A;Acommon in clinvarTypical
- rs1801198TCN2 · 30,615,623G;GSome increase in peripheral neuropathy risk in older adults taking folateWorth knowing
- rs2283873TCN2 · 30,617,309G;Gcommon genotypeTypical
- rs10418TCN2 · 30,626,965C;Ccommon in clinvarTypical
- rs2229874LIMK2 · 31,267,789G;Gcommon in complete genomicsTypical
- rs9609421SLC5A1 · 32,065,510A;Acommon in complete genomicsTypical
- rs9621532SYN3 · 32,688,525A;Acommon in complete genomicsTypical
- rs9609643TIMP3 · 32,855,072G;Gcommon in complete genomicsTypical
- rs9862TIMP3 · 32,857,293T;Tcommon in clinvarTypical
- rs11547635TIMP3 · 32,857,305C;Ccommon in clinvarTypical
- rs13057534,463,801A;Acommon in complete genomicsTypical
- rs2071746HMOX1 · 35,380,679A;AnormalTypical
- rs2071747HMOX1 · 35,381,192G;Gcommon in complete genomicsTypical
- rs2003813APOL2 · 36,232,947C;Ccommon in complete genomicsTypical
- rs2157249APOL2 · 36,234,993T;Tcommon in complete genomicsTypical
- rs73885319APOL1 · 36,265,860G;G~6x higher risk for end-stage renal diseaseVery important
- rs60910145APOL1 · 36,265,988G;G~6x higher risk for end-stage renal diseaseVery important
- rs71785313APOL1 · 36,266,000-;-~6x higher risk for end-stage renal diseaseVery important
- rs5756130MIR6819 · 36,288,285C;Ccommon genotypeTypical
- rs2269529MYH9 · 36,288,308T;Tcommon in clinvarTypical
- rs11912763MYH9 · 36,288,676G;Gcommon in complete genomicsTypical
- rs4821480MYH9 · 36,299,201T;Tcommon in complete genomicsTypical
- rs2032487MYH9 · 36,299,382T;Tcommon in complete genomicsTypical
- rs4821481MYH9 · 36,299,896T;Tcommon in complete genomicsTypical
- rs5750248MYH9 · 36,306,846C;Ccommon in complete genomicsTypical
- rs2413396MYH9 · 36,312,039C;Ccommon in clinvarTypical
- rs5750250MYH9 · 36,312,438A;Acommon in complete genomicsTypical
- rs3752462MYH9 · 36,314,138T;Tcommon in clinvarTypical
- rs5750285LOC105373021 · 36,708,203C;CBetter response to lithium treatmentTypical
- rs855791TMPRSS6 · 37,066,896G;GnormalTypical
- rs4820268TMPRSS6 · 37,073,551G;Gcommon in clinvarTypical
- rs3218253IL2RB · 37,148,770G;Gcommon/normalTypical
- rs743777IL2RB · 37,155,567A;ANo summary available.Typical
- rs229526C1QTNF6 · 37,185,382G;Gcommon in complete genomicsTypical
- rs2239774RAC2 · 37,241,613G;Gcommon in clinvarTypical
- rs1215790437,586,005A;Acommon genotypeTypical
- rs8135665SLC16A8 · 38,080,269C;Ccommon in clinvarTypical
- rs2267369PLA2G6 · 38,169,340C;Ccommon in clinvarTypical
- rs1534891CSNK1E · 38,299,094C;CNo summary available.Typical
- rs2072797SUN2 · 38,738,202C;CnormalTypical
- rs8177832APOBEC3G · 39,081,561A;Acommon genotypeTypical
- rs5421139,291,479G;Gcommon on affy axiom dataTypical
- rs4894ATF4 · 39,521,510A;AnormalTypical
- rs9623117TNRC6B · 40,056,115C;C1.1x increased risk for prostate cancerTypical
- rs12484776TNRC6B · 40,256,869A;ANormal Risk of UF for JapaneseTypical
- rs20551EP300 · 41,152,004A;Acommon in clinvarTypical
- rs2228314SREBF2 · 41,880,738C;C2.03x risk of osteoarthritisWorth knowing
- rs6002530SREBF2 · 41,906,460A;Acommon in complete genomicsTypical
- rs12169962CYP2D6 · 42,126,310C;Ccommon in complete genomicsTypical
- rs1135840LOC102723722 · 42,126,611G;GHomozygous for CYP2D6 variants (non-CYP2D6*1)Worth knowing
- rs28371733LOC102723722 · 42,126,914G;GHomozygous for non-functioning CYP2D6*4H variant.Important
- rs16947LOC102723722 · 42,127,941A;Ga common variantTypical
- rs28371717LOC102723722 · 42,128,308C;Ccommon in complete genomicsTypical
- rs3892097LOC102723722 · 42,128,945T;TCYP2D6 poor metabolizer; many associations related to drug metabolismImportant
- rs5030865LOC102723722 · 42,129,033A;ACYP2D6*8 inactive type homozygoteWorth knowing
- rs5030655LOC102723722 · 42,129,084-;-CYP2D6*6 poor metabolizer phenotypeImportant
- rs1065852LOC102723722 · 42,130,692A;AHomozygous for CYP2D6 decreased or non-functioning variants; possibly less response to some drugs, including tamoxifenImportant
- rs769258LOC102723722 · 42,130,761C;Ccommon in complete genomicsTypical
- rs28624811LOC102723722 · 42,131,531G;GNo summary available.Typical
- rs1080987LOC102723722 · 42,132,199C;Ccommon in complete genomicsTypical
- rs1080985LOC107984152 · 42,132,375G;Ga common variantTypical
- rs1807314CYP2D7 · 42,142,219A;Acommon in complete genomicsTypical
- rs1800457CYB5R3 · 42,628,265G;Gcommon in clinvarTypical
- rs575916743,104,206T;THigher prostate cancer riskWorth knowing
- rs8140172EFCAB6 · 43,808,439C;Ccommon genotypeTypical
- rs738409PNPLA3 · 43,928,847G;Ghigher odds of alcoholic liver disease, increased liver fatImportant
- rs6006460PNPLA3 · 43,946,294G;Tlower liver triglyceride (fat) levelsMinor
- rs16992796ARHGAP8 · 44,787,134A;Acommon in complete genomicsTypical
- rs600741345,034,435C;Ccommon in complete genomicsTypical
- rs4253623PPARA · 46,154,203A;AnormalTypical
- rs1800206PPARA · 46,218,377C;Ccommon in complete genomicsTypical
- rs4253778PPARA · 46,234,737G;Gcommon in complete genomicsTypical
- rs11090865TRMU · 46,335,792T;TModifier variant; some impact in rare casesImportant
- rs6007897CELSR1 · 46,384,624T;Tcommon in complete genomicsTypical
- rs9615362CELSR1 · 46,399,244C;Ccommon in complete genomicsTypical
- rs962718347,888,765G;Gcommon on affy axiom dataTypical
- rs1305408548,234,372G;Gcommon genotypeTypical
- rs17000918C22orf34 · 49,418,853C;CNo summary available.Typical
- rs2837244849,957,323G;Gcommon on affy axiom dataTypical
- rs140523SCO2 · 50,524,353C;Ccommon in clinvarTypical
- rs5770917CHKB-CPT1B · 50,578,924C;C>1.4x increased risk for narcolepsyTypical
- rs6151429ARSA · 50,625,049C;Cpseudoarylsulfatase A deficiency (possible)Important
- rs743616ARSA · 50,625,611G;Gcommon in clinvarTypical
- rs2071421ARSA · 50,625,988T;Tcommon in clinvarTypical
- rs74315472ARSA · 50,626,618A;Amiscalled by 23andMe; otherwise, when correct, Metachromatic leukodystrophy alleleImportant
- rs9616915SHANK3 · 50,679,152T;Tcommon in clinvarTypical
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.