rs2064689
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2064689(A;A) |
| Make rs2064689(A;G) |
| Make rs2064689(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 67187327 |
| Gene | IL23R |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2064689 |
| dbSNP (classic) | rs2064689 |
| ClinGen | rs2064689 |
| ebi | rs2064689 |
| HLI | rs2064689 |
| Exac | rs2064689 |
| Gnomad | rs2064689 |
| Varsome | rs2064689 |
| LitVar | rs2064689 |
| Map | rs2064689 |
| PheGenI | rs2064689 |
| Biobank | rs2064689 |
| 1000 genomes | rs2064689 |
| hgdp | rs2064689 |
| ensembl | rs2064689 |
| geneview | rs2064689 |
| scholar | rs2064689 |
| rs2064689 | |
| pharmgkb | rs2064689 |
| gwascentral | rs2064689 |
| openSNP | rs2064689 |
| 23andMe | rs2064689 |
| SNPshot | rs2064689 |
| SNPdbe | rs2064689 |
| MSV3d | rs2064689 |
| GWAS Ctlg | rs2064689 |
| GMAF | 0.3081 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs2064689 |
| PubMedID | [PMID 17804789 ]
|
| Condition | Crohn's disease |
| Gene | IL23R |
| Risk Allele | |
| pValue | 1.00E-008 |
| OR | 1.38 |
| 95% CI | 1.23-1.53 |
[PMID 17068223] A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
[PMID 20369022] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.
[PMID 21304977] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.
