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rs368269558(C;C)

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common/normal

Is a	genotype
of	rs368269558
Gene	DHCR7
Chromosome	11
Position	71,441,330
mentioned	by

0

Good

Geno	Mag	Summary
(C;C)	0	common/normal
(C;T)	3	Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation

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Is a genotype