RS146296049 HMGCS2

Health Risk Chr 1:119757423
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Associated Conditions
3-hydroxy-3-methylglutaryl-CoA synthase deficiency
Inborn genetic diseases
3-hydroxy-3-methylglutaryl-CoA synthase deficiency
Inborn genetic diseases
Other Variants in HMGCS2
rs137852636 rs137852637 rs137852638 rs137852639 rs28937320 rs137852640 rs796051979 rs144744634 rs142637231 rs773364048
Ask Dr. Hemsworth about this variant