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Variant (rsID / SNP)

rs12363178

OR52N4

rs12363178 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR52N4. Location: chromosome 11, position 5,776,595. The table records no clinical significance for this variant.

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Reference-table entries

OR52N4Not classified
Variant type
missense_variant
Chromosome / position
11:5776595
HGVS
NM_001005175.5,c.625T>G,p.Trp209Gly
Allele change
Missense_W209G

Public references

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