Gene entry
KCNK9
potassium two pore domain channel subfamily K member 9
- Chromosome
- 8
- Cytoband
- 8q24.3
- Variants (rsID)
- 29
KCNK9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8q24.3). Its official name is “potassium two pore domain channel subfamily K member 9”. The reference table lists 29 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs121908332Pathogenicsingle nucleotide variantBirk-Barel syndrome
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.
