RS377686388 ETFDH
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What This Variant Does
"CLNSIG=5
Associated Conditions
Multiple acyl-CoA dehydrogenase deficiency
Glutaric acidemia type 2C
Inborn genetic diseases
Multiple acyl-CoA dehydrogenase deficiency
Multiple acyl-CoA dehydrogenase deficiency
Glutaric acidemia type 2C
Inborn genetic diseases
Multiple acyl-CoA dehydrogenase deficiency
Other Variants in ETFDH