Variant (rsID / SNP)
rs11583410
rs11583410 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2B11. Location: chromosome 1, position 247,614,896. The table records no clinical significance for this variant.
Reference-table entries
OR2B11Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:247614896
- HGVS
- NM_001004492.2,c.389T>G,p.Ile130Ser
- Allele change
- Missense_I130S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
