RS763494292 HMGCL

Health Risk Chr 1:23820545
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What This Variant Does
"CLNSIG=5
Associated Conditions
Deficiency of hydroxymethylglutaryl-CoA lyase
Inborn genetic diseases
Deficiency of hydroxymethylglutaryl-CoA lyase
Deficiency of hydroxymethylglutaryl-CoA lyase
Inborn genetic diseases
Deficiency of hydroxymethylglutaryl-CoA lyase
Other Variants in HMGCL
rs752137615 rs121964997 rs121964998 rs786205431 rs727503963 rs771024022 rs886046312 rs886046313 rs778868742 rs568718845
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