rs121908978(G;G)

common in clinvar

Is a	genotype
of	rs121908978
Gene	SLC37A4
Chromosome	11
Position	119,029,287
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;G)	3	Carrier of a glycogen storage disease type Ib mutation
(G;G)	0	common in clinvar