RS138058572 ACADVL
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Myopathy
Rhabdomyolysis
Very long chain acyl-CoA dehydrogenase deficiency
Myopathy
Rhabdomyolysis
Very long chain acyl-CoA dehydrogenase deficiency
Other Variants in ACADVL