Rs12037606
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs12037606 |
| hapmap | rs12037606 |
| hgdp | rs12037606 |
| ensembl | rs12037606 |
| gopubmed | rs12037606 |
| scholar | rs12037606 |
| rs12037606 | |
| pharmgkb | rs12037606 |
| hgvbaseg2p | rs12037606 |
| medrefsnp | rs12037606 |
| 23andMe | rs12037606 |
| SNP Nexus |
| Chromosome | 1 |
| Orientation | plus |
| Position | 171165024 |
| Genotype | Effect |
|---|---|
| rs12037606(A;A) | 1.5x risk of Crohn's disease |
| rs12037606(A;G) | 1.2x risk of Crohn's disease |
| rs12037606(G;G) | normal |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs12037606(A;A) | 1.5x risk of Crohn's disease | |
| Rs12037606(A;G) | 1.2x risk of Crohn's disease | |
| Rs12037606(C;C) | 00 | |
| Rs12037606(G;G) | normal |
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]
| ? | (A;A) (A;G) (G;G) |
|---|---|
|
| |
