RS121434280 ACADM

Health Risk Chr 1:75732723 snv missense variant
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What This Variant Does
"aka c.199T&gt
Associated Conditions
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Inborn genetic diseases
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0.1%
Other Variants in ACADM
rs77931234 rs1225471006 rs121434274 rs121434275 rs121434277 rs387906297 rs864621963 rs121434278 rs121434279 rs121434282
Ask Dr. Hemsworth about this variant