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Gene entry

DBH

dopamine beta-hydroxylase

Chromosome
9
Cytoband
9q34.2
Variants (rsID)
50

DBH is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q34.2). Its official name is “dopamine beta-hydroxylase”. The reference table lists 50 variants (rsID) for this gene.

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Clinically classified variants

14 reference-table entries with clinical significance.

  • rs1611115Associationsingle nucleotide variantDopamine beta-hydroxylase polymorphism
  • rs1108580Benignsingle nucleotide variantDopamine beta-hydroxylase deficiency
  • rs129914Benignsingle nucleotide variantDopamine beta-hydroxylase deficiency
  • rs13306301Benignsingle nucleotide variantDopamine beta-hydroxylase deficiency
  • rs1611131Benignsingle nucleotide variantDopamine beta-hydroxylase deficiency
  • rs35465867Benignsingle nucleotide variantDopamine beta-hydroxylase deficiency
  • rs5322Benignsingle nucleotide variantDopamine beta-hydroxylase deficiency
  • rs77905Benignsingle nucleotide variantDopamine beta-hydroxylase deficiency
  • rs7862391Benignsingle nucleotide variantDopamine beta-hydroxylase deficiency
  • rs3025380Likely benignsingle nucleotide variantDopamine beta-hydroxylase deficiency
  • rs74853476Pathogenicsingle nucleotide variantDopamine beta-hydroxylase deficiency
  • rs145059403Uncertain significancesingle nucleotide variantDopamine beta-hydroxylase deficiency
  • rs200798319Uncertain significancesingle nucleotide variantDopamine beta-hydroxylase deficiency
  • rs75215331Not classifiedsingle nucleotide variantDopamine beta-hydroxylase 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.