rs11676348
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11676348(C;C) |
| Make rs11676348(C;T) |
| Make rs11676348(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 218145423 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11676348 |
| dbSNP (classic) | rs11676348 |
| ClinGen | rs11676348 |
| ebi | rs11676348 |
| HLI | rs11676348 |
| Exac | rs11676348 |
| Gnomad | rs11676348 |
| Varsome | rs11676348 |
| LitVar | rs11676348 |
| Map | rs11676348 |
| PheGenI | rs11676348 |
| Biobank | rs11676348 |
| 1000 genomes | rs11676348 |
| hgdp | rs11676348 |
| ensembl | rs11676348 |
| geneview | rs11676348 |
| scholar | rs11676348 |
| rs11676348 | |
| pharmgkb | rs11676348 |
| gwascentral | rs11676348 |
| openSNP | rs11676348 |
| 23andMe | rs11676348 |
| SNPshot | rs11676348 |
| SNPdbe | rs11676348 |
| MSV3d | rs11676348 |
| GWAS Ctlg | rs11676348 |
| GMAF | 0.4568 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21297633 ]
|
| Trait | |
| Title | Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 |
| Risk Allele | T |
| P-val | 1E-10 |
| Odds Ratio | 1.0700 [1.03-1.11] |
[PMID 26071399] Identification of a Common Variant with Potential Pleiotropic Effect on Risk of Inflammatory Bowel Disease and Colorectal Cancer
