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Gene entry

ACADS

acyl-CoA dehydrogenase short chain

Chromosome
12
Cytoband
12q24.31
Variants (rsID)
18

ACADS is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q24.31). Its official name is “acyl-CoA dehydrogenase short chain”. The reference table lists 18 variants (rsID) for this gene.

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Clinically classified variants

17 reference-table entries with clinical significance.

  • rs1799958Benignsingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs201420791Benignsingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs3916Benignsingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs9204Benignsingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs1800556Conflicting interpretationssingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs28940874Conflicting interpretationssingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs368469075Conflicting interpretationssingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs371550264Conflicting interpretationssingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs61732144Conflicting interpretationssingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs774815274Conflicting interpretationssingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs121908003Pathogenicsingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs121908006Pathogenicsingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs28940875Pathogenicsingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs28941773Pathogenicsingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs57443665Pathogenicsingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase|See cases
  • rs749491616Pathogenicsingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase
  • rs199717731Uncertain significancesingle nucleotide variantDeficiency of butyryl-CoA dehydrogenase

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.