rs121908001(G;G)

common in clinvar

Is a	genotype
of	rs121908001
Gene	ATP7B
Chromosome	13
Position	51,960,198
mentioned	by

Magnitude

0

Repute

Good

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