Variant (rsID / SNP)
rs11724
rs11724 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2I1P. Location: chromosome 6, position 29,521,319. The table records no clinical significance for this variant.
Reference-table entries
OR2I1PNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:29521319
- HGVS
- NM_001396058.1,c.324C>G,p.Ser108Ser
Associated conditions / phenotypes
Celiac Disease 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.