rs770516374(C;G)
From SNPedia
Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma |
Is a | genotype |
of | rs770516374 |
Gene | PMEL |
Chromosome | 12 |
Position | 55,957,191 |
mentioned | by |
Magnitude | 5.5 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;G) | 5.5 | Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma |
see text at main rs-page