Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11209026
rs11209026
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.900 GeneticVariation GWASDB A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. 22936669

2013
dbSNP: rs11209026
rs11209026
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.900 GeneticVariation GWASDB A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. 22412388

2012
dbSNP: rs11209026
rs11209026
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.900 GeneticVariation GWASDB One is SNP rs11209026 in exon 9 of IL23R for association with Crohn's disease, which is predicted to be probably damaging by PolyPhen2. 22293688

2012
dbSNP: rs11209026
rs11209026
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.900 GeneticVariation GWASDB Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463

2010
dbSNP: rs11209026
rs11209026
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.900 GeneticVariation GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394

2008
dbSNP: rs11209026
rs11209026
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.900 GeneticVariation GWASDB Systematic association mapping identifies NELL1 as a novel IBD disease gene. 17684544

2007
dbSNP: rs11209026
rs11209026
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.900 GeneticVariation GWASDB Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4. 17447842

2007
dbSNP: rs11209026
rs11209026
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.900 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007