Variant (rsID / SNP)

rs12054944

rs12054944 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WWC1. Location: chromosome 5, position 167,850,748. The table records no clinical significance for this variant.

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Reference-table entries

WWC1Not classified

Variant type: synonymous_variant
Chromosome / position: 5:167850748
HGVS: NM_001161661.2,c.1485A>G,p.Ser495Ser
Allele change: Synonymous_S495S

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.