Gene entry
HADH
hydroxyacyl-CoA dehydrogenase
- Chromosome
- 4
- Cytoband
- 4q25
- Variants (rsID)
- 15
HADH is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q25). Its official name is “hydroxyacyl-CoA dehydrogenase”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs4956145Benignsingle nucleotide variantDeficiency of 3-hydroxyacyl-CoA dehydrogenase
- rs760202Benignsingle nucleotide variantHyperinsulinemic hypoglycemia, familial, 4|Deficiency of 3-hydroxyacyl-CoA dehydrogenase
- rs1051519Conflicting interpretationssingle nucleotide variantMonogenic diabetes|Deficiency of 3-hydroxyacyl-CoA dehydrogenase|Hyperinsulinemic hypoglycemia, familial, 4|Deficiency of 3-hydroxyacyl-CoA dehydrogenase|Hyperinsulinemic hypoglycemia, familial, 4
- rs140413151Conflicting interpretationssingle nucleotide variantMonogenic diabetes|Deficiency of 3-hydroxyacyl-CoA dehydrogenase|Hyperinsulinemic hypoglycemia, familial, 4|Deficiency of 3-hydroxyacyl-CoA dehydrogenase|Hyperinsulinemic hypoglycemia, familial, 4
- rs146036912Conflicting interpretationssingle nucleotide variantDeficiency of 3-hydroxyacyl-CoA dehydrogenase|Hyperinsulinemic hypoglycemia, familial, 4
- rs61735992Conflicting interpretationssingle nucleotide variantMonogenic diabetes|Deficiency of 3-hydroxyacyl-CoA dehydrogenase|Hyperinsulinemic hypoglycemia, familial, 4
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.