rs7551188
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7551188(C;C) |
| Make rs7551188(C;T) |
| Make rs7551188(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 24946709 |
| Gene | LOC105376878, RUNX3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7551188 |
| dbSNP (classic) | rs7551188 |
| ClinGen | rs7551188 |
| ebi | rs7551188 |
| HLI | rs7551188 |
| Exac | rs7551188 |
| Gnomad | rs7551188 |
| Varsome | rs7551188 |
| LitVar | rs7551188 |
| Map | rs7551188 |
| PheGenI | rs7551188 |
| Biobank | rs7551188 |
| 1000 genomes | rs7551188 |
| hgdp | rs7551188 |
| ensembl | rs7551188 |
| geneview | rs7551188 |
| scholar | rs7551188 |
| rs7551188 | |
| pharmgkb | rs7551188 |
| gwascentral | rs7551188 |
| openSNP | rs7551188 |
| 23andMe | rs7551188 |
| SNPshot | rs7551188 |
| SNPdbe | rs7551188 |
| MSV3d | rs7551188 |
| GWAS Ctlg | rs7551188 |
| GMAF | 0.4844 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23266558] |
| Trait | Crohn's disease |
| Title | A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population. |
| Risk Allele | T |
| P-val | 9E-6 |
| Odds Ratio | 1.18 [1.10-1.28] |
