Variant (rsID / SNP)

rs56170708

rs56170708 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WNK2. Location: chromosome 9, position 96,010,036. The table records no clinical significance for this variant.

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Reference-table entries

WNK2Not classified

Variant type: missense_variant
Chromosome / position: 9:96010036
HGVS: NM_001282394.3,c.1754G>A,p.Gly585Glu
Allele change: Missense_G585E

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.