Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10758669
rs10758669
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016
dbSNP: rs10758669
rs10758669
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		C 0.850 GeneticVariation GWASCAT Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463

2010
dbSNP: rs10758669
rs10758669
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		C 0.850 GeneticVariation GWASCAT Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394

2008
dbSNP: rs10889677
rs10889677
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 GeneticVariation GWASCAT Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007
dbSNP: rs13361189
rs13361189
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 GeneticVariation GWASCAT Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. 17554261

2007
dbSNP: rs1893217
rs1893217
PTPN2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.850 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015
dbSNP: rs1893217
rs1893217
PTPN2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.850 GeneticVariation GWASCAT Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463

2010
dbSNP: rs2201841
rs2201841
IL23R ; C1orf141
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 GeneticVariation GWASCAT Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007
dbSNP: rs3024505
rs3024505
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908

2017
dbSNP: rs3024505
rs3024505
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		A 0.850 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015
dbSNP: rs3024505
rs3024505
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		T 0.850 GeneticVariation GWASCAT Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463

2010
dbSNP: rs3810936
rs3810936
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		C 0.850 GeneticVariation GWASCAT Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463

2010
dbSNP: rs76418789
rs76418789
IL23R ; C1orf141
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
dbSNP: rs76418789
rs76418789
IL23R ; C1orf141
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.850 GeneticVariation GWASCAT Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations. 23850713

2014
dbSNP: rs1000113
rs1000113
IRGM
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		T 0.840 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007
dbSNP: rs7848647
rs7848647
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.840 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016
dbSNP: rs10883365
rs10883365
LINC01475
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.830 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007
dbSNP: rs10883365
rs10883365
LINC01475
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 GeneticVariation GWASCAT Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. 17554261

2007
dbSNP: rs2076756
rs2076756
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.830 GeneticVariation GWASCAT A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. 22936669

2013
dbSNP: rs2076756
rs2076756
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.830 GeneticVariation GWASCAT A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. 22412388

2012
dbSNP: rs2076756
rs2076756
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.830 GeneticVariation GWASCAT Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463

2010
dbSNP: rs2076756
rs2076756
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 GeneticVariation GWASCAT Systematic association mapping identifies NELL1 as a novel IBD disease gene. 17684544

2007
dbSNP: rs2076756
rs2076756
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 GeneticVariation GWASCAT Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 17435756

2007
dbSNP: rs3197999
rs3197999
APEH ; MST1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908

2017
dbSNP: rs3197999
rs3197999
APEH ; MST1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016