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Gene entry

ACADSB

acyl-CoA dehydrogenase short/branched chain

Chromosome
10
Cytoband
10q26.13
Variants (rsID)
12

ACADSB is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q26.13). Its official name is “acyl-CoA dehydrogenase short/branched chain”. The reference table lists 12 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs188094280Conflicting interpretationssingle nucleotide variantDeficiency of 2-methylbutyryl-CoA dehydrogenase|Seizure
  • rs58639322Conflicting interpretationssingle nucleotide variantDeficiency of 2-methylbutyryl-CoA dehydrogenase
  • rs72839755Likely benignsingle nucleotide variantDeficiency of 2-methylbutyryl-CoA dehydrogenase
  • rs1345480688Pathogenicsingle nucleotide variantDeficiency of 2-methylbutyryl-CoA dehydrogenase
  • rs137852649Pathogenicsingle nucleotide variantDeficiency of 2-methylbutyryl-CoA dehydrogenase
  • rs201877440Pathogenicsingle nucleotide variantDeficiency of 2-methylbutyryl-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.