Rs2902440
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs2902440 |
| hapmap | rs2902440 |
| hgdp | rs2902440 |
| ensembl | rs2902440 |
| gopubmed | rs2902440 |
| scholar | rs2902440 |
| rs2902440 | |
| pharmgkb | rs2902440 |
| hgvbaseg2p | rs2902440 |
| medrefsnp | rs2902440 |
| 23andMe | rs2902440 |
| SNP Nexus |
| Chromosome | 1 |
| Orientation | plus |
| Position | 67443503 |
| Genotype | Effect |
|---|---|
| rs2902440(A;A)* | ? |
| rs2902440(A;G)* | ? |
| rs2902440(G;G)* | ? |
| GWAS | |
|---|---|
| SNP | rs2902440 |
| PubMedID | [PMID 17804789] |
| Condition | Crohn's disease |
| Gene | IL23R |
| Risk Allele | |
| pValue | 1.00E-008 |
| OR | 1.38 |
| 95% CI | 1.23-1.53 |
| Neighbor | rs1004819 |
| Distance | 702 |
| PharmGKB | PA162356490 |
| Name | |
| Annotation | GWAS results: Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci (Initial Sample Size: 382 trios; Replication Sample Size: 521 trios, 750 cases, 828 controls). This variant is associated with Crohn's disease. This variant is associated with Crohn's disease. |
| Gene | IL23R |
| Featue | |
| Evidence | PubMed ID:17804789; Web Resource:http://www.genome.gov/gwastudies/ |
| Drugs | |
| Diseases | Crohn Disease |
| Curation Level | Non-Curated |
