Have questions? Visit https://www.reddit.com/r/SNPedia

rs748713829(C;T)

From SNPedia
Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma
Is agenotype
ofrs748713829
GenePMEL
Chromosome12
Position55,957,309
mentionedby
Magnitude5.5
ReputeBad
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