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Variant (rsID / SNP)

rs2512226

OR10D3

rs2512226 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR10D3. Location: chromosome 11, position 124,056,787. The table records no clinical significance for this variant.

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Reference-table entries

OR10D3Not classified
Variant type
missense_variant
Chromosome / position
11:124056787
HGVS
NM_001355213.3,c.811G>A,p.Val271Met
Allele change
Missense_V271M

Public references

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