rs273900
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;T) | 0 | common in complete genomics |
| Make rs273900(C;C) |
| Make rs273900(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 132358913 |
| Gene | LOC553103 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs273900 |
| dbSNP (classic) | rs273900 |
| ClinGen | rs273900 |
| ebi | rs273900 |
| HLI | rs273900 |
| Exac | rs273900 |
| Gnomad | rs273900 |
| Varsome | rs273900 |
| LitVar | rs273900 |
| Map | rs273900 |
| PheGenI | rs273900 |
| Biobank | rs273900 |
| 1000 genomes | rs273900 |
| hgdp | rs273900 |
| ensembl | rs273900 |
| geneview | rs273900 |
| scholar | rs273900 |
| rs273900 | |
| pharmgkb | rs273900 |
| gwascentral | rs273900 |
| openSNP | rs273900 |
| 23andMe | rs273900 |
| SNPshot | rs273900 |
| SNPdbe | rs273900 |
| MSV3d | rs273900 |
| GWAS Ctlg | rs273900 |
| GMAF | 0.4417 |
| Max Magnitude | 0 |
[PMID 18668679] rs272893 and rs273900 are associated with Crohn's disease (OR 2.16; 95% CI 1.21-3.59 and OR 2.40; 95% CI 1.43-4.05)
[PMID 17476680] Genetic susceptibility has a more important role in pediatric-onset Crohn's disease than in adult-onset Crohn's disease.
