RS796051963 ETFDH

Health Risk Chr 4:158684671
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What This Variant Does
"CLNSIG=5
Associated Conditions
Multiple acyl-CoA dehydrogenase deficiency
Inborn genetic diseases
Multiple acyl-CoA dehydrogenase deficiency
Inborn genetic diseases
Other Variants in ETFDH
rs121964953 rs2150304327 rs121964954 rs121964955 rs121964956 rs387907170 rs377656387 rs398124151 rs398124152 rs398124153
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