rs137853280(C;G)
From SNPedia
Unaffected carrier of a Wilson disease mutation |
Is a | genotype |
of | rs137853280 |
Gene | ATP7B |
Chromosome | 13 |
Position | 51,965,034 |
mentioned | by |
Magnitude | 3 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;G) | 3 | Unaffected carrier of a Wilson disease mutation |
(G;G) | 0 | common in clinvar |
(G;T) | 3 | Unaffected carrier of a Wilson disease mutation |
Unaffected in absence of a second ATP7B gene mutation; see links via main rs-page.