|| common in complete genomics
|?|| (A;A) (A;G) (G;G) ||28|
|| [PMID 18587394]
|| Crohn's disease
|| Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease
| Risk Allele
| Odds Ratio
|| 1.33 [NR]
|Desc||INFLAMMATORY BOWEL DISEASE 19; IBD19|
] Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.
[PMID 20106866] Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.
[PMID 22065112] The JAK2 variant rs10758669 in Crohn's disease: altering the intestinal barrier as one mechanism of action.