RS752317877 HADHA

Health Risk Chr 2:26212590
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What This Variant Does
"CLNSIG=4
Associated Conditions
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Inborn genetic diseases
Mitochondrial trifunctional protein deficiency
HADHA-related disorder
Mitochondrial trifunctional protein deficiency 1
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Inborn genetic diseases
Mitochondrial trifunctional protein deficiency
HADHA-related disorder
Mitochondrial trifunctional protein deficiency 1
Other Variants in HADHA
rs137852769 rs137852770 rs786205088 rs781222705 rs137852771 rs1574600309 rs137852772 rs137852774 rs137852775 rs147103714
Ask Dr. Hemsworth about this variant