rs6601764
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 2 | 1.52x increased risk of developing Crohn's disease |
| (C;T) | 1.5 | 1.16x increased risk of developing Crohn's disease |
| (T;T) | 1 | Normal risk of developing Crohn's disease |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 3820350 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6601764 |
| dbSNP (classic) | rs6601764 |
| ClinGen | rs6601764 |
| ebi | rs6601764 |
| HLI | rs6601764 |
| Exac | rs6601764 |
| Gnomad | rs6601764 |
| Varsome | rs6601764 |
| LitVar | rs6601764 |
| Map | rs6601764 |
| PheGenI | rs6601764 |
| Biobank | rs6601764 |
| 1000 genomes | rs6601764 |
| hgdp | rs6601764 |
| ensembl | rs6601764 |
| geneview | rs6601764 |
| scholar | rs6601764 |
| rs6601764 | |
| pharmgkb | rs6601764 |
| gwascentral | rs6601764 |
| openSNP | rs6601764 |
| 23andMe | rs6601764 |
| SNPshot | rs6601764 |
| SNPdbe | rs6601764 |
| MSV3d | rs6601764 |
| GWAS Ctlg | rs6601764 |
| GMAF | 0.3669 |
| Max Magnitude | 2 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
rs6601764 has been reported in a large study to be associated with Crohn's disease.
The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 1.16 (CI 1.01-1.33), and for homozygotes, 1.52 (CI 1.28-1.80). [PMID 17554300
]
