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Variant (rsID / SNP)

rs6591536

OR5A1

rs6591536 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR5A1. Location: chromosome 11, position 59,211,188. The table records no clinical significance for this variant.

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Reference-table entries

OR5A1Not classified
Variant type
missense_variant
Chromosome / position
11:59211188
HGVS
NM_001004728.2,c.547G>A,p.Asp183Asn
Allele change
Missense_D183N

Public references

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