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Gene entry

KCNN4

potassium calcium-activated channel subfamily N member 4

Chromosome
19
Cytoband
19q13.31
Variants (rsID)
10

KCNN4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.31). Its official name is “potassium calcium-activated channel subfamily N member 4”. The reference table lists 10 variants (rsID) for this gene.

Clinically classified variants

1 reference-table entries with clinical significance.

  • rs774455945Pathogenicsingle nucleotide variantDehydrated hereditary stomatocytosis 2

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.