rs397514631(A;A)

common in clinvar

Is a	genotype
of	rs397514631
Gene	PYGM
Chromosome	11
Position	64,759,747
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	3	Carrier of a McArdle disease mutation
(G;G)	5	McArdle disease (also known as glycogen storage disease type V)