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Gene entry

CTNNA3

catenin alpha 3

Chromosome
10
Cytoband
10q21.3
Variants (rsID)
357

CTNNA3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q21.3). Its official name is “catenin alpha 3”. The reference table lists 357 variants (rsID) for this gene.

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Clinically classified variants

8 reference-table entries with clinical significance.

  • rs115276158Benignsingle nucleotide variantArrhythmogenic right ventricular dysplasia 13
  • rs143682596Benignsingle nucleotide variantArrhythmogenic right ventricular dysplasia 13
  • rs2105702Benignsingle nucleotide variantArrhythmogenic right ventricular dysplasia 13
  • rs41274090Benignsingle nucleotide variantArrhythmogenic right ventricular dysplasia 13
  • rs77165728Conflicting interpretationssingle nucleotide variantArrhythmogenic right ventricular dysplasia 13
  • rs146777494Uncertain significancesingle nucleotide variantArrhythmogenic right ventricular dysplasia 13
  • rs192848934Uncertain significancesingle nucleotide variantArrhythmogenic right ventricular dysplasia 13
  • rs201306690Uncertain significancesingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Arrhythmogenic right ventricular dysplasia 13

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.