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Variant (rsID / SNP)

rs12792184

OR8A1

rs12792184 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR8A1. Location: chromosome 11, position 124,440,617. The table records no clinical significance for this variant.

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Reference-table entries

OR8A1Not classified
Variant type
missense_variant
Chromosome / position
11:124440617
HGVS
NM_001005194.2,c.602C>T,p.Ser201Leu
Allele change
Missense_S218L

Public references

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