Variant (rsID / SNP)

rs73122754

rs73122754 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WFDC3. Location: chromosome 20, position 44,417,593. The table records no clinical significance for this variant.

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Reference-table entries

WFDC3Not classified

Variant type: missense_variant
Chromosome / position: 20:44417593
HGVS: NM_080614.2,c.188G>T,p.Arg63Leu
Allele change: Missense_R63L

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.