RS142761835 IVD

Health Risk Chr 15:40410699
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=255
Associated Conditions
Isovaleryl-CoA dehydrogenase deficiency
IVD-related disorder
Inborn genetic diseases
Isovaleryl-CoA dehydrogenase deficiency
IVD-related disorder
Inborn genetic diseases
Other Variants in IVD
rs121434284 rs121434285 rs34695403 rs28940889 rs398123679 rs398123680 rs398123681 rs398123682 rs398123683 rs398123684
Ask Dr. Hemsworth about this variant