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i5012679

From SNPedia
23andMe dataI5012679
23andMe searchI5012679
opensnpI5012679
Gene (via rs)PMM2
aliasrs80338701
Rs_StabilizedOrientationplus
RsGeno Mag Summary
(A;C) 3 Carrier of a congenital disorder of glycosylation type I mutation
(C;C) 0 common in clinvar

rs80338701

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