rs121907998(G;T)
From SNPedia
Carrier of a Wilson disease mutation |
Is a | genotype |
of | rs121907998 |
Gene | ATP7B |
Chromosome | 13 |
Position | 51,961,849 |
mentioned | by |
Magnitude | 3 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(G;T) | 3 | Carrier of a Wilson disease mutation |
(T;T) | 0 | common in clinvar |
Unaffected in absence of a second ATP7B gene mutation; see links via main rs-page