rs104894212(G;G)

common in clinvar

Is a	genotype
of	rs104894212
Gene	DHCR7
Chromosome	11
Position	71,438,966
Merged from	Rs28939698
mentioned	by

Magnitude

0

Repute

Good

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