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rs143312232(G;G)

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common in clinvar

Is a	genotype
of	rs143312232
Gene	DHCR7
Chromosome	11
Position	71,441,392
mentioned	by

0

Good

Geno	Mag	Summary
(A;C)	3	Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
(C;G)	3	Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
(G;G)	0	common in clinvar

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Is a genotype