Variant (rsID / SNP)

rs880054

rs880054 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WNK1. Location: chromosome 12, position 988,558. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

WNK1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:988558
Cytoband: 12p13.33
HGVS: NM_018979.4(WNK1):c.2374-181C>T
Allele change: Silent

Associated conditions / phenotypes

Neuropathy, hereditary sensory and autonomic, type 2A|Pseudohypoaldosteronism type 2C

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.