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rs756974126(G;G)

From SNPedia
common/normal
Is agenotype
ofrs756974126
GenePMEL
Chromosome12
Position55,957,284
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 5.5 Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma
(G;G) 0 common/normal

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