Variant (rsID / SNP)

rs200182836

rs200182836 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WNK4. Location: chromosome 17, position 40,939,393. Clinical significance in the table: Benign.

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Reference-table entries

WNK4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:40939393
Cytoband: 17q21.2
HGVS: NM_032387.5(WNK4):c.1574G>A (p.Arg525His)
Allele change: Missense_R189H

Associated conditions / phenotypes

Pseudohypoaldosteronism type 2B

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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