Variant (rsID / SNP)

rs55997156

rs55997156 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WNK4. Location: chromosome 17, position 40,939,342. Clinical significance in the table: Likely benign.

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Reference-table entries

WNK4Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:40939342
Cytoband: 17q21.2
HGVS: NM_032387.5(WNK4):c.1523G>A (p.Arg508His)
Allele change: Missense_R172H

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.