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Gene entry

WNK1

WNK lysine deficient protein kinase 1

Chromosome
12
Cytoband
12p13.33
Variants (rsID)
33

WNK1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12p13.33). Its official name is “WNK lysine deficient protein kinase 1”. The reference table lists 33 variants (rsID) for this gene.

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Clinically classified variants

11 reference-table entries with clinical significance.

  • rs11833299Benignsingle nucleotide variantPseudohypoaldosteronism type 2C|Neuropathy, hereditary sensory and autonomic, type 2A|Pseudohypoaldosteronism type 2C
  • rs12828016Benignsingle nucleotide variantPseudohypoaldosteronism type 2C|Neuropathy, hereditary sensory and autonomic, type 2A|Neuropathy, hereditary sensory and autonomic, type 2A|Pseudohypoaldosteronism type 2C
  • rs150532648Benignsingle nucleotide variantVariant of unknown significance|Pseudohypoaldosteronism type 2C|Neuropathy, hereditary sensory and autonomic, type 2A|Pseudohypoaldosteronism type 2C
  • rs17755373Benignsingle nucleotide variantPseudohypoaldosteronism type 2C|Pseudohypoaldosteronism type 2C|Neuropathy, hereditary sensory and autonomic, type 2A
  • rs2286007Benignsingle nucleotide variantPseudohypoaldosteronism type 2C|Neuropathy, hereditary sensory and autonomic, type 2A|Pseudohypoaldosteronism type 2C|Neuropathy, hereditary sensory and autonomic, type 2A
  • rs880054Benignsingle nucleotide variantNeuropathy, hereditary sensory and autonomic, type 2A|Pseudohypoaldosteronism type 2C
  • rs956868Benignsingle nucleotide variantPseudohypoaldosteronism type 2C|Neuropathy, hereditary sensory and autonomic, type 2A|Pseudohypoaldosteronism type 2C|Neuropathy, hereditary sensory and autonomic, type 2A
  • rs72648621Conflicting interpretationssingle nucleotide variantPseudohypoaldosteronism type 2C|Neuropathy, hereditary sensory and autonomic, type 2A|Pseudohypoaldosteronism type 2C
  • rs72650720Conflicting interpretationssingle nucleotide variantPseudohypoaldosteronism type 2C|Pseudohypoaldosteronism type 2C|Neuropathy, hereditary sensory and autonomic, type 2A
  • rs72647373Likely benignsingle nucleotide variantNeuropathy, hereditary sensory and autonomic, type 2A|Pseudohypoaldosteronism type 2C
  • rs111033591Pathogenicsingle nucleotide variantNeuropathy, hereditary sensory and autonomic, type 2A|Pseudohypoaldosteronism type 2C|Neuropathy, hereditary sensory and autonomic, type 2A

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.