rs28938174(A;T)

Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation

Is a	genotype
of	rs28938174
Gene	DHCR7
Chromosome	11
Position	71,442,319
mentioned	by

Magnitude

3

Repute

Bad

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

see Smith-Lemli-Opitz syndrome