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Variant (rsID / SNP)

rs7948009

OR52N1

rs7948009 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR52N1. Location: chromosome 11, position 5,809,548. The table records no clinical significance for this variant.

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Reference-table entries

OR52N1Not classified
Variant type
missense_variant
Chromosome / position
11:5809548
HGVS
NM_001001913.2,c.499C>T,p.Arg167Cys
Allele change
Missense_R167C

Public references

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