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i5901102

From SNPedia
23andMe dataI5901102
23andMe searchI5901102
opensnpI5901102
Gene (via rs)MSH6

aliasrs63751077
Rs_StabilizedOrientationplus
RsGeno Mag Summary
(A;C) 6 Lynch syndrome, pathogenic mutation
(C;C) 0 common in clinvar

rs63751077