rs76151636(G;G)

common in clinvar

Is a	genotype
of	rs76151636
Gene	ATP7B
Chromosome	13
Position	51,944,145
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	3	Carrier of a Wilson's disease mutation
(T;T)	5.7	Wilson's disease; variable age of onset