Chromosome 21
101 well-documented SNPs on chromosome 21, in order of position (GRCh38).
- rs7278737LIPI · 14,109,044G;TNo summary available.Typical
- rs7283442LIPI · 14,144,655A;ANo summary available.Typical
- rs2823256LOC101927745 · 15,412,387A;Anormal risk of Crohn's disease in KoreansTypical
- rs10446073CHODL · 17,820,455G;GNo summary available.Typical
- rs2824721TMPRSS15 · 18,297,801A;ANo summary available.Typical
- rs11088859NCAM2 · 21,317,024G;Gcommon on affy axiom dataTypical
- rs282852023,770,802G;G1.35x major depressive disorder riskMinor
- rs1700123925,630,065C;Ccommon on affy axiom dataTypical
- rs63750264APP · 25,891,784C;TAlzheimer's disease mutationVery important
- rs63750671APP · 25,891,858C;GSignificantly increased risk for early-onset Alzheimer's diseaseVery important
- rs63750064APP · 25,897,605C;TSignificantly increased risk for Alzheimer's diseaseVery important
- rs193922916APP · 25,897,619A;Asignificantly increased alzheimer's riskVery important
- rs63750847APP · 25,897,620T;Tresistance to Alzheimer's diseaseVery important
- rs281865161APP · 25,897,626GA;TCAlzheimer's disease, familialVery important
- rs364048APP · 26,171,723T;Tcommon genotypeTypical
- rs22903826,833,110G;Gcommon/normalTypical
- rs2738ADAMTS1 · 26,836,585C;Ccommon/normalTypical
- rs997749927,362,678C;Tcommon in complete genomicsTypical
- rs145209327,372,037A;Gcommon in complete genomicsTypical
- rs2832387LOC54073 · 29,518,574G;Gcommon in complete genomicsTypical
- rs2832407GRIK1 · 29,595,188C;Ctopiramate may work to reduce heavy drinking best for this genotypeWorth knowing
- rs726002GRIK1 · 29,678,973G;GNo summary available.Typical
- rs930540630,013,925A;Acommon in complete genomicsTypical
- rs13048019TIAM1 · 31,545,981C;Ccommon on affy axiom dataTypical
- rs7277748SOD1 · 31,659,661A;Acommon in complete genomicsTypical
- rs2070424SOD1 · 31,667,007A;Acommon in complete genomicsTypical
- rs1041740SOD1 · 31,667,849T;TSlight increase in cardiovascular risk?Minor
- rs17880487SOD1 · 31,668,917C;Ccommon in clinvarTypical
- rs283360732,008,727G;GNo summary available.Typical
- rs2833991LOC105377136 · 32,890,379A;Acommon genotypeTypical
- rs762237LOC105372785 · 33,035,869C;Ccommon in complete genomicsTypical
- rs2229207IFNAR2 · 33,241,945T;Tcommon in complete genomicsTypical
- rs2834167IL10RB · 33,268,483A;A2.67x increased risk for systemic sclerosisWorth knowing
- rs3171425IL10RB · 33,296,442A;Acommon in clinvarTypical
- rs2234916KCNE2 · 34,370,500A;Acommon in complete genomicsTypical
- rs74315448KCNE2 · 34,370,648T;Tcommon in clinvarTypical
- rs16991654KCNE2 · 34,370,656T;Tcommon in clinvarTypical
- rs1805128KCNE1 · 34,449,382C;Ccommon in complete genomicsTypical
- rs74315445KCNE1 · 34,449,409C;Ccommon in clinvarTypical
- rs17846179KCNE1 · 34,449,523C;TNo summary available.Typical
- rs1805127KCNE1 · 34,449,523C;Tslight (1.4x) increase in risk for atrial fibrillationMinor
- rs16992204LINC00160 · 34,738,904T;Tcommon genotypeTypical
- rs2253319RUNX1 · 34,815,749C;Tcommon in complete genomicsTypical
- rs9976946LOC102724584 · 34,835,765T;TNo summary available.Typical
- rs283481235,161,365C;Ccommon in complete genomicsTypical
- rs16993221LOC100506403 · 35,477,121A;Acommon genotypeTypical
- rs1143663CBR1 · 36,070,377G;Gcommon in complete genomicsTypical
- rs2835285CBR3 · 36,135,469G;Gcommon in complete genomicsTypical
- rs4987121CBR3 · 36,146,381A;Acommon in complete genomicsTypical
- rs1056892CBR3 · 36,146,408G;Gcommon in clinvarTypical
- rs2835342CHAF1B · 36,414,379G;Gcommon in complete genomicsTypical
- rs219780LOC105369301 · 36,461,009C;Ccommon in complete genomicsTypical
- rs219778LOC105369301 · 36,462,343A;Acommon in complete genomicsTypical
- rs11701483DYRK1A · 37,427,806A;ANo summary available.Typical
- rs2154545DYRK1A · 37,498,982A;Gcommon in complete genomicsTypical
- rs2070995KCNJ6 · 37,714,662C;TNo summary available.Typical
- rs283606137,952,931C;CNo summary available.Typical
- rs3746876KCNJ15 · 38,299,525C;Ccommon in complete genomicsTypical
- rs989554ERG · 38,415,005A;ANo summary available.Typical
- rs7275212ERG · 38,480,628A;Acommon in complete genomicsTypical
- rs9979250LOC400867 · 38,911,809C;Ccommon genotypeTypical
- rs224294439,093,252A;A0.7x lower odds of ankylosing spondylitis, according to 23andMeMinor
- rs2150410BRWD1 · 39,197,853A;Acommon in complete genomicsTypical
- rs1735151IGSF5 · 39,751,374C;Ccommon in complete genomicsTypical
- rs2837960LINC00323 · 41,139,991G;G2.3x rheumatoid arthritis riskWorth knowing
- rs12329760TMPRSS2 · 41,480,570C;Ccommon/normalTypical
- rs13049286RIPK4 · 41,756,639T;Tcommon in clinvarTypical
- rs2839471UMODL1 · 42,134,346C;CnormalTypical
- rs4148102ABCG1 · 42,221,237G;Gcommon in complete genomicsTypical
- rs998166042,317,828G;Gcommon genotypeTypical
- rs928302TMPRSS3 · 42,389,975C;Ccommon in complete genomicsTypical
- rs6586282CBS · 43,058,387C;Ccommon in clinvarTypical
- rs1789953CBS · 43,062,826C;Ccommon in clinvarTypical
- rs5742905CBS · 43,063,074G;Gpossible miscall in Ancestry V2.0 datasets; otherwise, Mild clinical homocystinuria which is responsive to vitamin B6Important
- rs234706CBS · 43,065,240A;A0.50 reduced risk of cleft lip / palate, 0.51 reduced risk of non-Hodgkin lymphoma. Increased responsiveness to homocysteine-lowering effects of folic acid.Worth knowing
- rs2298758CBS · 43,065,417G;Gcommon in complete genomicsTypical
- rs285014643,080,476C;Ccommon in complete genomicsTypical
- rs3761381CRYAA · 43,168,145C;Ccommon genotypeTypical
- rs9306160RRP1B · 43,687,681T;T0.75x (reduced) risk for metastasis in LN-/ER+ breast cancer patientsMinor
- rs2071152TRAPPC10 · 44,083,240A;ANo summary available.Typical
- rs878081AIRE · 44,288,394C;Ccommon in clinvarTypical
- rs1055311AIRE · 44,289,685C;Ccommon in clinvarTypical
- rs1133779AIRE · 44,297,667T;Tcommon in clinvarTypical
- rs2838554TRPM2 · 44,364,749G;GNo summary available.Typical
- rs12329790CBS · 44,483,184A;ANo summary available.Typical
- rs235326ITGB2 · 44,891,898A;Acommon in clinvarTypical
- rs235330ITGB2 · 44,894,992A;Acommon in complete genomicsTypical
- rs2230528ITGB2 · 44,900,398C;Ccommon in clinvarTypical
- rs9983887ITGB2 · 44,903,541G;Gcommon in clinvarTypical
- rs2070947ITGB2 · 44,920,928A;Acommon in clinvarTypical
- rs12483377COL18A1 · 45,511,195A;Abenign polymorphism; no significant effectMinor
- rs7499COL18A1 · 45,512,414G;Gcommon in clinvarTypical
- rs1051266SLC19A1 · 45,537,880T;Tcommon in clinvarTypical
- rs481914345,704,264G;Gcommon in complete genomicsTypical
- rs1053312COL6A1 · 46,003,475A;GNo summary available.Typical
- rs1697881046,068,418C;Ccommon genotypeTypical
- rs2839110COL6A2 · 46,119,046A;ANo summary available.Typical
- rs1042917COL6A2 · 46,125,854G;Gcommon in clinvarTypical
- rs2249057PCNT · 46,353,189C;Ccommon in clinvarTypical
- rs2073376PCNT · 46,431,839A;Acommon in clinvarTypical
- rs2073380PCNT · 46,443,844A;Acommon 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.