Variant (rsID / SNP)

rs417425

rs417425 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR52D1, OR51B5. Location: chromosome 11, position 5,510,284. The table records no clinical significance for this variant.

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Reference-table entries

OR52D1Not classified

Variant type: synonymous_variant
Chromosome / position: 11:5510284
HGVS: NM_001005163.2,c.348A>G,p.Ser116Ser
Allele change: Silent

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.