Variant (rsID / SNP)
rs2853083
rs2853083 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR5AK2. Location: chromosome 11, position 56,756,664. The table records no clinical significance for this variant.
Reference-table entries
OR5AK2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:56756664
- HGVS
- NM_001005323.1,c.276G>A,p.Met92Ile
- Allele change
- Missense_M92I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.