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Variant (rsID / SNP)

rs6591699

OR5D16

rs6591699 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR5D16. Location: chromosome 11, position 55,606,302. The table records no clinical significance for this variant.

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Reference-table entries

OR5D16Not classified
Variant type
synonymous_variant
Chromosome / position
11:55606302
HGVS
NM_001005496.1,c.75G>T,p.Leu25Leu
Allele change
Synonymous_L25L

Public references

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