Gene entry
IVD
isovaleryl-CoA dehydrogenase
- Chromosome
- 15
- Cytoband
- 15q15.1
- Variants (rsID)
- 21
IVD is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q15.1). Its official name is “isovaleryl-CoA dehydrogenase”. The reference table lists 21 variants (rsID) for this gene.
Clinically classified variants
13 reference-table entries with clinical significance.
- rs138427412Benignsingle nucleotide variantIsovaleryl-CoA dehydrogenase deficiency
- rs2075624Benignsingle nucleotide variantIsovaleryl-CoA dehydrogenase deficiency
- rs369694967Conflicting interpretationssingle nucleotide variantIsovaleryl-CoA dehydrogenase deficiency
- rs398123679Conflicting interpretationssingle nucleotide variantIsovaleryl-CoA dehydrogenase deficiency
- rs750569823Conflicting interpretationssingle nucleotide variantIsovaleryl-CoA dehydrogenase deficiency
- rs796051983Likely pathogenicsingle nucleotide variantIsovaleryl-CoA dehydrogenase deficiency
- rs121434285Pathogenicsingle nucleotide variantIsovaleric acidemia, type I|Isovaleryl-CoA dehydrogenase deficiency
- rs142761835Pathogenicsingle nucleotide variantIsovaleryl-CoA dehydrogenase deficiency
- rs28940889Pathogenicsingle nucleotide variantIsovaleryl-CoA dehydrogenase deficiency|Inborn genetic diseases
- rs398123682PathogenicDeletionIsovaleryl-CoA dehydrogenase deficiency
- rs765815516Pathogenicsingle nucleotide variantIsovaleryl-CoA dehydrogenase deficiency
- rs150855952Uncertain significancesingle nucleotide variantIsovaleryl-CoA dehydrogenase deficiency
- rs367891946Uncertain significancesingle nucleotide variantIsovaleryl-CoA dehydrogenase deficiency
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.