rs768729972(-;A)
From SNPedia
Carrier of a Wilson disease mutation |
Is a | genotype |
of | rs768729972 |
Gene | ATP7B |
Chromosome | 13 |
Position | 51,958,500 |
mentioned | by |
Magnitude | 3 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(-;A) | 3 | Carrier of a Wilson disease mutation |
Unaffected in absence of a second ATP7B gene mutation; see links via main rs-page