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Variant (rsID / SNP)

rs8181512

OR52N2

rs8181512 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR52N2. Location: chromosome 11, position 5,842,356. The table records no clinical significance for this variant.

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Reference-table entries

OR52N2Not classified
Variant type
missense_variant
Chromosome / position
11:5842356
HGVS
NM_001005174.3,c.791A>G,p.His264Arg
Allele change
Missense_H264R

Public references

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