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Variant (rsID / SNP)

rs10839632

OR10A2

rs10839632 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR10A2. Location: chromosome 11, position 6,891,704. The table records no clinical significance for this variant.

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Reference-table entries

OR10A2Not classified
Variant type
missense_variant
Chromosome / position
11:6891704
HGVS
NM_001004460.2,c.719T>C,p.Ile240Thr
Allele change
Missense_I240T

Public references

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