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Gene entry

KCNB1

potassium voltage-gated channel subfamily B member 1

Chromosome
20
Cytoband
20q13.13
Variants (rsID)
32

KCNB1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20q13.13). Its official name is “potassium voltage-gated channel subfamily B member 1”. The reference table lists 32 variants (rsID) for this gene.

Clinically classified variants

3 reference-table entries with clinical significance.

  • rs112735799Benignsingle nucleotide variantDevelopmental and epileptic encephalopathy, 26
  • rs34280195Benignsingle nucleotide variantDevelopmental and epileptic encephalopathy, 26
  • rs587777849Pathogenicsingle nucleotide variantDevelopmental and epileptic encephalopathy, 26

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.