RS58639322 ACADSB

Health Risk Chr 10:123040605
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What This Variant Does
"[OMIM:?]
Associated Conditions
Deficiency of 2-methylbutyryl-CoA dehydrogenase
Inborn genetic diseases
Deficiency of 2-methylbutyryl-CoA dehydrogenase
Inborn genetic diseases
Other Variants in ACADSB
rs387906409 rs137852649 rs188094280 rs147936696 rs760791287 rs374420253 rs150619709 rs886046780 rs886046781 rs202191462
Ask Dr. Hemsworth about this variant