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Variant (rsID / SNP)

rs150532648

WNK1

rs150532648 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WNK1. Location: chromosome 12, position 992,587. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

WNK1Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
12:992587
Cytoband
12p13.33
HGVS
NM_018979.4(WNK1):c.3516A>G (p.Ile1172Met)
Allele change
Missense_I1424M

Associated conditions / phenotypes

Variant of unknown significance|Pseudohypoaldosteronism type 2C|Neuropathy, hereditary sensory and autonomic, type 2A|Pseudohypoaldosteronism type 2C

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.