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Gene entry

ACADVL

acyl-CoA dehydrogenase very long chain

Chromosome
17
Cytoband
17p13.1
Variants (rsID)
29

ACADVL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p13.1). Its official name is “acyl-CoA dehydrogenase very long chain”. The reference table lists 29 variants (rsID) for this gene.

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Clinically classified variants

24 reference-table entries with clinical significance.

  • rs144996066Benignsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs28934585Benignsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs76547988Benignsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs77763289Benignsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs113994169Conflicting interpretationssingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs138834083Conflicting interpretationssingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs140629318Conflicting interpretationssingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs148584617Conflicting interpretationssingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs200771970Conflicting interpretationssingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs202217537Conflicting interpretationssingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs372592554Conflicting interpretationssingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs727503791Conflicting interpretationssingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs79125791Conflicting interpretationssingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs113690956Pathogenicsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs113994167Pathogenicsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency|Very long chain fatty acid accumulation
  • rs113994171Pathogenicsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs118204014Pathogenicsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs118204016Pathogenicsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency|Abnormality of circulating enzyme level|Rhabdomyolysis
  • rs118204018Pathogenicsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs2309689Pathogenicsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs369560930Pathogenicsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs398123083Pathogenicsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs727503788Pathogenicsingle nucleotide variantVery long chain acyl-CoA dehydrogenase deficiency
  • rs753108198PathogenicDeletionVery long chain acyl-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.