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rs770516374(C;C)

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common/normal

Is a	genotype
of	rs770516374
Gene	PMEL
Chromosome	12
Position	55,957,191
mentioned	by

0

Good

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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Is a genotype