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i5037891

From SNPedia
23andMe dataI5037891
23andMe searchI5037891
opensnpI5037891
Gene (via rs)MSH6

aliasrs587779209
Rs_StabilizedOrientationplus
RsGeno Mag Summary
(-;T) 6 Lynch syndrome, pathogenic mutation
(T;T) 0 common in clinvar

rs587779209