RS80338855 DHCR7

Health Risk Chr 11:71441347
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What This Variant Does
"CLNSIG=5
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