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Variant (rsID / SNP)

rs11231529

OR5W2

rs11231529 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR5W2. Location: chromosome 11, position 55,681,336. The table records no clinical significance for this variant.

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Reference-table entries

OR5W2Not classified
Variant type
synonymous_variant
Chromosome / position
11:55681336
HGVS
NM_001001960.1,c.723C>T,p.Cys241Cys
Allele change
Synonymous_C241C

Public references

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