RS765191836 SRD5A3

Health Risk Chr 4:55367628
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Congenital disorder of glycosylation
Inborn genetic diseases
Congenital disorder of glycosylation
Other Variants in SRD5A3
rs587776521 rs267607093 rs267607095 rs267607092 rs267607094 rs869320736 rs398124401 rs201123766 rs376944136 rs797046008
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