rs104894213(A;G)

Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation

Is a	genotype
of	rs104894213
Gene	DHCR7
Chromosome	11
Position	71,441,400
mentioned	by

Magnitude

3

Repute

Bad

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

see Smith-Lemli-Opitz syndrome