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Variant (rsID / SNP)

rs12338899

OR13D1

rs12338899 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR13D1. Location: chromosome 9, position 107,457,725. The table records no clinical significance for this variant.

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Reference-table entries

OR13D1Not classified
Variant type
synonymous_variant
Chromosome / position
9:107457725
HGVS
NM_001004484.2,c.927G>A,p.Leu309Leu
Allele change
Synonymous_L341L

Public references

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