rs121907992(G;G)

common in clinvar

Is a	genotype
of	rs121907992
Gene	ATP7B
Chromosome	13
Position	51,937,583
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;G)	3	Carrier of a Wilson disease mutation
(G;G)	0	common in clinvar