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rs142410496(A;G)

From SNPedia
Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma
Is agenotype
ofrs142410496
GenePMEL
Chromosome12
Position55,957,137
mentionedby
Magnitude5.5
ReputeBad
Geno Mag Summary
(A;A) 0 common/normal
(A;G) 5.5 Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma

see text at main rs-page