Variant (rsID / SNP)
rs6728493
rs6728493 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR6B3. Location: chromosome 2, position 240,981,262. The table records no clinical significance for this variant.
Reference-table entries
OR6B3Not classified
- Variant type
- downstream_gene_variant
- Chromosome / position
- 2:240981262
- HGVS
- NM_173351.2,c.*3232T>G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.