Rs6601764
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs6601764 |
| hapmap | rs6601764 |
| hgdp | rs6601764 |
| ensembl | rs6601764 |
| gopubmed | rs6601764 |
| scholar | rs6601764 |
| rs6601764 | |
| pharmgkb | rs6601764 |
| hgvbaseg2p | rs6601764 |
| medrefsnp | rs6601764 |
| 23andMe | rs6601764 |
| SNP Nexus |
| Chromosome | 10 |
| Orientation | plus |
| Position | 3852541 |
| Genotype | Effect |
|---|---|
| rs6601764(C;C) | 1.5x risk |
| rs6601764(C;T) | 1.1x risk |
| rs6601764(T;T) | normal |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs6601764(C;C) | 1.5x risk | |
| Rs6601764(C;T) | 1.1x risk | |
| Rs6601764(T;T) | 00 | normal |
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]
| ? | (C;C) (C;T) (T;T) |
|---|---|
|
| |
