RS200620279 ACAD8
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Deficiency of isobutyryl-CoA dehydrogenase
Inborn genetic diseases
ACAD8-related disorder
Deficiency of isobutyryl-CoA dehydrogenase
Inborn genetic diseases
ACAD8-related disorder
Other Variants in ACAD8