rs104886033(A;A)

common in clinvar

Is a	genotype
of	rs104886033
Gene	DHCR7
Chromosome	11
Position	71,444,952
mentioned	by

Magnitude

0

Repute

Good

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