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rs142410496(A;A)

From SNPedia
common/normal
Is agenotype
ofrs142410496
GenePMEL
Chromosome12
Position55,957,137
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common/normal
(A;G) 5.5 Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma