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i5901124

From SNPedia
23andMe dataI5901124
23andMe searchI5901124
opensnpI5901124
Gene (via rs)MSH6
aliasrs587776705
Rs_StabilizedOrientationplus
RsGeno Mag Summary
(-;GTG) 5 Variant of uncertain significance; possible Lynch syndrome mutation
(GTG;GTG) 0 common in clinvar

rs587776705

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