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rs3214759(C;C)

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common in clinvar

Is a	genotype
of	rs3214759
Gene	LOC100507443, CRYGB
Chromosome	2
Position	208,146,054
mentioned	by

0

Good

Geno	Mag	Summary
(-;C)	1.5	probably actually benign, but one report links to cataracts
(C;C)	0	common in clinvar

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Is a genotype