rs121907993(C;G)
From SNPedia
| Carrier of a Wilson disease mutation |
| Is a | genotype |
| of | rs121907993 |
| Gene | ATP7B |
| Chromosome | 13 |
| Position | 51,949,772 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;G) | 3 | Carrier of a Wilson disease mutation |
Unaffected in absence of a second ATP7B gene mutation; see links via main rs-page
