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rs17118154(C;C)

From SNPedia
common/normal
Is agenotype
ofrs17118154
GenePMEL
Chromosome12
Position55,957,193
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common/normal
(C;G) 5.5 Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma

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