RS751995154 ACADVL

Health Risk Chr 17:7224011
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What This Variant Does
"CLNSIG=5
Associated Conditions
Myopathy
Rhabdomyolysis
Very long chain acyl-CoA dehydrogenase deficiency
Inborn genetic diseases
ACADVL-related disorder
Very long chain acyl-CoA dehydrogenase deficiency
Myopathy
Rhabdomyolysis
Very long chain acyl-CoA dehydrogenase deficiency
Inborn genetic diseases
ACADVL-related disorder
Very long chain acyl-CoA dehydrogenase deficiency
Other Variants in ACADVL
rs113690956 rs118204014 rs387906249 rs387906251 rs118204015 rs118204017 rs118204018 rs118204016 rs113994169 rs2309689
Ask Dr. Hemsworth about this variant