rs80338701(C;C)

common in clinvar

Is a	genotype
of	rs80338701
Gene	PMM2
Chromosome	16
Position	8,811,088
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;C)	3	Carrier of a congenital disorder of glycosylation type I mutation
(C;C)	0	common in clinvar