Variant (rsID / SNP)
rs2741804
rs2741804 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2D2. Location: chromosome 11, position 6,913,127. The table records no clinical significance for this variant.
Reference-table entries
OR2D2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:6913127
- HGVS
- NM_003700.1,c.605T>C,p.Met202Thr
- Allele change
- Missense_M202T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
