Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7539328
rs7539328
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223

2006
dbSNP: rs1105267
rs1105267
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223

2006
dbSNP: rs10489629
rs10489629
IL23R ; C1orf141
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223

2006
dbSNP: rs2066845
rs2066845
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation GWASDB Systematic association mapping identifies NELL1 as a novel IBD disease gene. 17684544

2007
dbSNP: rs2066845
rs2066845
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007
dbSNP: rs2066844
rs2066844
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation GWASDB Systematic association mapping identifies NELL1 as a novel IBD disease gene. 17684544

2007
dbSNP: rs2066844
rs2066844
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007
dbSNP: rs2241880
rs2241880
ATG16L1 ; SCARNA5
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: rs2241880
rs2241880
ATG16L1 ; SCARNA5
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.900 GeneticVariation GWASDB Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 17435756

2007
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
dbSNP: rs2066847
rs2066847
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.890 GeneticVariation GWASDB Systematic association mapping identifies NELL1 as a novel IBD disease gene. 17684544

2007
dbSNP: rs7517847
rs7517847
IL23R ; C1orf141
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.880 GeneticVariation GWASDB Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 17435756

2007
dbSNP: rs2542151
rs2542151
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.880 GeneticVariation GWASDB Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. 17554261

2007
dbSNP: rs2542151
rs2542151
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.880 GeneticVariation GWASDB Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007
dbSNP: rs2201841
rs2201841
IL23R ; C1orf141
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 GeneticVariation GWASDB 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 GWASDB Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. 17554261

2007
dbSNP: rs10889677
rs10889677
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007
dbSNP: rs1000113
rs1000113
IRGM
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		T 0.840 GeneticVariation GWASDB Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007
dbSNP: rs5743293
rs5743293
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.830 GeneticVariation GWASDB 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 GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

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

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

2007