Gene entry
HADHB
hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta
- Chromosome
- 2
- Cytoband
- 2p23.3
- Variants (rsID)
- 11
HADHB is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p23.3). Its official name is “hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs56902571Benignsingle nucleotide variantMitochondrial trifunctional protein deficiency
- rs57709136Benignsingle nucleotide variantMitochondrial trifunctional protein deficiency
- rs57969630Benignsingle nucleotide variantMitochondrial trifunctional protein deficiency
- rs72851534Benignsingle nucleotide variantMitochondrial trifunctional protein deficiency
- rs72851542Benignsingle nucleotide variantMitochondrial trifunctional protein deficiency
- rs121913132Likely pathogenicsingle nucleotide variantMitochondrial trifunctional protein deficiency
- rs121913133Likely pathogenicsingle nucleotide variantMitochondrial trifunctional protein 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.