RS779709646 DHCR7

Health Risk Chr 11:71435664
Upload your DNA to see your genotype for this variant.
What This Variant Does
"c.1139G&gt
Associated Conditions
Smith-Lemli-Opitz syndrome
Inborn genetic diseases
Smith-Lemli-Opitz syndrome
Inborn genetic diseases
Other Variants in DHCR7
rs2539221742 rs2539221237 rs28938174 rs121909764 rs104894212 rs80338853 rs104894213 rs80338859 rs80338860 rs61757582
Ask Dr. Hemsworth about this variant