RS387907170 ETFDH
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What This Variant Does
"CLNSIG=5
Associated Conditions
Glutaric acidemia iic
late-onset
Inborn genetic diseases
Multiple acyl-CoA dehydrogenase deficiency
Glutaric acidemia type 2C
Glutaric acidemia iic
late-onset
Inborn genetic diseases
Multiple acyl-CoA dehydrogenase deficiency
Glutaric acidemia type 2C
Other Variants in ETFDH