Rs10761659
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs10761659 |
| hapmap | rs10761659 |
| hgdp | rs10761659 |
| ensembl | rs10761659 |
| gopubmed | rs10761659 |
| scholar | rs10761659 |
| rs10761659 | |
| pharmgkb | rs10761659 |
| hgvbaseg2p | rs10761659 |
| medrefsnp | rs10761659 |
| 23andMe | rs10761659 |
| SNP Nexus |
| Chromosome | 10 |
| Orientation | plus |
| Position | 64115569 |
| Genotype | Effect |
|---|---|
| rs10761659(A;A) | 1.5x risk |
| rs10761659(A;G) | 1.2x risk |
| rs10761659(G;G) | normal |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs10761659(A;A) | 00 | 1.5x risk |
| Rs10761659(A;G) | 1.2x risk | |
| Rs10761659(G;G) | normal |
The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.23 (CI 1.05-1.45), and for homozygotes, 1.55 (CI 1.3-1.84). [PMID 17554300]
| ? | (A;A) (A;G) (G;G) |
|---|---|
|
| |
[PMID 19174780] Confirmation of multiple Crohn's disease susceptibility loci in a large Dutch-Belgian cohort
Related to INFLAMMATORY BOWEL DISEASE 15; IBD15
according to omim 612255. See also
