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Variant (rsID / SNP)

rs866347

OR6A2

rs866347 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR6A2. Location: chromosome 11, position 6,816,778. The table records no clinical significance for this variant.

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Reference-table entries

OR6A2Not classified
Variant type
synonymous_variant
Chromosome / position
11:6816778
HGVS
NM_003696.3,c.162T>C,p.Ser54Ser
Allele change
Synonymous_S54S

Public references

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