rs748713829(C;T)
From SNPedia
| Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma |
| Is a | genotype |
| of | rs748713829 |
| Gene | PMEL |
| Chromosome | 12 |
| Position | 55,957,309 |
| mentioned | by |
| Magnitude | 5.5 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common/normal |
| (C;T) | 5.5 | Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma |
see text at main rs-page
