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Variant (rsID / SNP)

rs7048527

WNK2

rs7048527 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WNK2. Location: chromosome 9, position 95,993,170. The table records no clinical significance for this variant.

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Reference-table entries

WNK2Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
9:95993170
HGVS
NM_001282394.3,c.855A>G,p.Thr285Thr
Allele change
Synonymous_T285T

Public references

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