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Gene entry

SCN3B

sodium voltage-gated channel beta subunit 3

Chromosome
11
Cytoband
11q24.1
Variants (rsID)
15

SCN3B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q24.1). Its official name is “sodium voltage-gated channel beta subunit 3”. The reference table lists 15 variants (rsID) for this gene.

Clinically classified variants

6 reference-table entries with clinical significance.

  • rs553042856Benignsingle nucleotide variant
  • rs72552198Benignsingle nucleotide variant
  • rs121918282Conflicting interpretationssingle nucleotide variantBrugada syndrome 7|Atrial fibrillation, familial, 16|Brugada syndrome|Cardiovascular phenotype
  • rs147205617Conflicting interpretationssingle nucleotide variantDeath in infancy|Cardiovascular phenotype|Cardiomyopathy|Brugada syndrome 7
  • rs587777555Uncertain significancesingle nucleotide variantBrugada syndrome 7
  • rs587777556Uncertain significancesingle nucleotide variantAtrial fibrillation, familial, 16|Brugada syndrome 7

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.