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rs142410496(A;A)

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common/normal

Is a	genotype
of	rs142410496
Gene	PMEL
Chromosome	12
Position	55,957,137
mentioned	by

0

Good

Geno	Mag	Summary
(A;A)	0	common/normal
(A;G)	5.5	Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma

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Is a genotype