rs121908000(C;T)
From SNPedia
| Carrier of a Wilson disease mutation |
| Is a | genotype |
| of | rs121908000 |
| Gene | ATP7B |
| Chromosome | 13 |
| Position | 51,958,543 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;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
