Variant (rsID / SNP)

rs12933084

rs12933084 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WFDC1. Location: chromosome 16, position 84,360,533. The table records no clinical significance for this variant.

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Reference-table entries

WFDC1Not classified

Variant type: missense_variant
Chromosome / position: 16:84360533
HGVS: NM_001282466.2,c.650A>G,p.Lys217Arg
Allele change: Missense_K217R

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.