From SNPedia
rs1793004 is a SNP in the
NELL1 gene that was found in a genome-wide association study to be associated with
Crohn's disease.
In several European populations, the most common allele, rs1793004(C), was associated with increased risk for Crohn's disease. Conversely, the odds ratio (pooled over several populations) for the minor allele, rs1793004(G), was 0.89 (CI: 0.69-1.14, p=0.0037).[PMID 17684544]
| ? | (C;C) (C;G) (G;G) |
|---|
 |
| PharmGKB | PA162356578 |
| Name | |
| Annotation | GWAS results: Systematic association mapping identifies NELL1 as a novel IBD disease gene (Initial Sample Size: 393 cases, 399 controls; Replication Sample Size: 2,920 cases, 1,961 controls, 1,248 trios). This variant is associated with Irritable bowel syndrome. |
| Gene | NELL1 |
| Featue | |
| Evidence | PubMed ID:17684544; Web Resource:http://www.genome.gov/gwastudies/ |
| Drugs | |
| Diseases | Colonic Diseases, Functional |
| Curation Level | Non-Curated |
