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rs148258956(C;C)

From SNPedia
common/normal
Is agenotype
ofrs148258956
GenePMEL
Chromosome12
Position55,957,329
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;C) 5.5 Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma
(C;C) 0 common/normal

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