rs10889676
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10889676(A;A) |
| Make rs10889676(A;C) |
| Make rs10889676(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 67256884 |
| Gene | IL23R |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10889676 |
| dbSNP (classic) | rs10889676 |
| ClinGen | rs10889676 |
| ebi | rs10889676 |
| HLI | rs10889676 |
| Exac | rs10889676 |
| Gnomad | rs10889676 |
| Varsome | rs10889676 |
| LitVar | rs10889676 |
| Map | rs10889676 |
| PheGenI | rs10889676 |
| Biobank | rs10889676 |
| 1000 genomes | rs10889676 |
| hgdp | rs10889676 |
| ensembl | rs10889676 |
| geneview | rs10889676 |
| scholar | rs10889676 |
| rs10889676 | |
| pharmgkb | rs10889676 |
| gwascentral | rs10889676 |
| openSNP | rs10889676 |
| 23andMe | rs10889676 |
| SNPshot | rs10889676 |
| SNPdbe | rs10889676 |
| MSV3d | rs10889676 |
| GWAS Ctlg | rs10889676 |
| GMAF | 0.365 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs10889676 |
| PubMedID | [PMID 17804789 ]
|
| Condition | Crohn's disease |
| Gene | IL23R |
| Risk Allele | |
| pValue | 1.00E-008 |
| OR | 1.38 |
| 95% CI | 1.23-1.53 |
