rs11465770
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | normal Crohn's Disease risk |
| (C;T) | 1.5 | possibly lower risk of Crohn's Disease (OR=0.30) |
| (T;T) | 1.5 | possibly lower risk of Crohn's Disease (OR=0.30) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 67168280 |
| Gene | IL23R |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11465770 |
| dbSNP (classic) | rs11465770 |
| ClinGen | rs11465770 |
| ebi | rs11465770 |
| HLI | rs11465770 |
| Exac | rs11465770 |
| Gnomad | rs11465770 |
| Varsome | rs11465770 |
| LitVar | rs11465770 |
| Map | rs11465770 |
| PheGenI | rs11465770 |
| Biobank | rs11465770 |
| 1000 genomes | rs11465770 |
| hgdp | rs11465770 |
| ensembl | rs11465770 |
| geneview | rs11465770 |
| scholar | rs11465770 |
| rs11465770 | |
| pharmgkb | rs11465770 |
| gwascentral | rs11465770 |
| openSNP | rs11465770 |
| 23andMe | rs11465770 |
| SNPshot | rs11465770 |
| SNPdbe | rs11465770 |
| MSV3d | rs11465770 |
| GWAS Ctlg | rs11465770 |
| GMAF | 0.0404 |
| Max Magnitude | 1.5 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
Contribution of rs11465788 in IL23R gene to Crohn's disease susceptibility and phenotype in Chinese population. [PMID 19700857] Found that T allele may be protective against Crohn's disease in Chinese.
