rs138659167(C;C)

common in clinvar

Is a	genotype
of	rs138659167
Gene	DHCR7
Chromosome	11
Position	71,435,840
mentioned	by

Magnitude

0

Repute

Good

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