rs12037606
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 2 | 1.52x risk of developing Crohn's disease |
| (A;G) | 1.5 | 1.22x risk of developing Crohn's disease |
| (C;C) | 0 | |
| (G;G) | 1 | Normal risk of developing Crohn's disease |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 172929262 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12037606 |
| dbSNP (classic) | rs12037606 |
| ClinGen | rs12037606 |
| ebi | rs12037606 |
| HLI | rs12037606 |
| Exac | rs12037606 |
| Gnomad | rs12037606 |
| Varsome | rs12037606 |
| LitVar | rs12037606 |
| Map | rs12037606 |
| PheGenI | rs12037606 |
| Biobank | rs12037606 |
| 1000 genomes | rs12037606 |
| hgdp | rs12037606 |
| ensembl | rs12037606 |
| geneview | rs12037606 |
| scholar | rs12037606 |
| rs12037606 | |
| pharmgkb | rs12037606 |
| gwascentral | rs12037606 |
| openSNP | rs12037606 |
| 23andMe | rs12037606 |
| SNPshot | rs12037606 |
| SNPdbe | rs12037606 |
| MSV3d | rs12037606 |
| GWAS Ctlg | rs12037606 |
| GMAF | 0.3388 |
| Max Magnitude | 2 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
rs12037606 has been reported in a large study to be associated with Crohn's disease.
The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with heterozygotes is 1.22 (CI 1.07-1.40), and for homozygotes, 1.52 (CI 1.28-1.82). [PMID 17554300
]
