rs7807268
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 2 | 1.4x risk for Crohn's disease |
| (C;G) | 2 | 1.3x risk for Crohn's disease |
| (G;G) | normal |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 148560956 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7807268 |
| dbSNP (classic) | rs7807268 |
| ClinGen | rs7807268 |
| ebi | rs7807268 |
| HLI | rs7807268 |
| Exac | rs7807268 |
| Gnomad | rs7807268 |
| Varsome | rs7807268 |
| LitVar | rs7807268 |
| Map | rs7807268 |
| PheGenI | rs7807268 |
| Biobank | rs7807268 |
| 1000 genomes | rs7807268 |
| hgdp | rs7807268 |
| ensembl | rs7807268 |
| geneview | rs7807268 |
| scholar | rs7807268 |
| rs7807268 | |
| pharmgkb | rs7807268 |
| gwascentral | rs7807268 |
| openSNP | rs7807268 |
| 23andMe | rs7807268 |
| SNPshot | rs7807268 |
| SNPdbe | rs7807268 |
| MSV3d | rs7807268 |
| GWAS Ctlg | rs7807268 |
| GMAF | 0.4931 |
| Max Magnitude | 2 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
rs7807268 has been reported in a large study to be associated with Crohn's disease.
The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.38 (CI 1.20-1.60), and for homozygotes, 1.47 (CI 1.24-1.74). [PMID 17554300
]
- Note: there is a slight amount of ambiguity over the orientation of this SNP information relative to the dbSNP entry.
