Rs11209002
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11209002 |
| PheGenI | rs11209002 |
| nextbio | rs11209002 |
| hapmap | rs11209002 |
| 1000 genomes | rs11209002 |
| hgdp | rs11209002 |
| ensembl | rs11209002 |
| gopubmed | rs11209002 |
| geneview | rs11209002 |
| scholar | rs11209002 |
| rs11209002 | |
| pharmgkb | rs11209002 |
| gwascentral | rs11209002 |
| openSNP | rs11209002 |
| 23andMe | rs11209002 |
| 23andMe all | rs11209002 |
| SNP Nexus | |
| SNPshot | rs11209002 |
| SNPdbe | rs11209002 |
| MSV3d | rs11209002 |
| Gene | C1orf141 |
| Chromosome | 1 |
| Orientation | plus |
| GMAF | 0.2189 |
| Position | 67590461 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs11209002(C;C) |
| Make rs11209002(C;T) |
| Make rs11209002(T;T) |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
| GWAS | |
|---|---|
| SNP | rs11209002 |
| PubMedID | [PMID 17804789] |
| Condition | Crohn's disease |
| Gene | IL23R |
| Risk Allele | |
| pValue | 2.00E-007 |
| OR | 2.56 |
| 95% CI | 1.75-3.70 |
| GET Evidence | |
|---|---|
| rs11209002 | |
| aa_change | |
| aa_change_short | |
| impact | pharmacogenetic |
| qualified_impact | Insufficiently evaluated pharmacogenetic |
| overall_frequency | 0.726562 |
| summary | |
