Gene entry
KCNA5
potassium voltage-gated channel subfamily A member 5
- Chromosome
- 12
- Cytoband
- 12p13.32
- Variants (rsID)
- 8
KCNA5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12p13.32). Its official name is “potassium voltage-gated channel subfamily A member 5”. The reference table lists 8 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs12720442Benignsingle nucleotide variantAtrial fibrillation, familial, 7
- rs17215402Benignsingle nucleotide variantAtrial fibrillation, familial, 7
- rs12720445Conflicting interpretationssingle nucleotide variantAtrial fibrillation, familial, 7|Brugada syndrome 1
- rs77281462Conflicting interpretationssingle nucleotide variantAtrial fibrillation, familial, 7
- rs121908591Uncertain significancesingle nucleotide variantAtrial fibrillation, familial, 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.