rs121907997(C;C)

common in clinvar

Is a	genotype
of	rs121907997
Gene	ATP7B
Chromosome	13
Position	51,958,369
mentioned	by

Magnitude

0

Repute

Good

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