Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2066843
rs2066843
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.710 GeneticVariation GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223

2006

dbSNP: rs2076756
rs2076756
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: rs5743289
rs5743289
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 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: rs17221417
rs17221417
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
G 0.810 GeneticVariation GWASDB Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007

dbSNP: rs2066845
rs2066845
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
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: rs2066847
rs2066847
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: rs5743293
rs5743293
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
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: rs540973741
rs540973741
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 GeneticVariation GWASDB Systematic association mapping identifies NELL1 as a novel IBD disease gene. 17684544

2007

dbSNP: rs199883290
rs199883290
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 GeneticVariation GWASDB Systematic association mapping identifies NELL1 as a novel IBD disease gene. 17684544

2007

dbSNP: rs2066845
rs2066845
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
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: rs2076756
rs2076756
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: rs5743289
rs5743289
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007

dbSNP: rs17221417
rs17221417
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007

dbSNP: rs2066842
rs2066842
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.790 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007

dbSNP: rs5743291
rs5743291
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.710 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007

dbSNP: rs17313265
rs17313265
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.710 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007

dbSNP: rs8057341
rs8057341
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007

dbSNP: rs8056611
rs8056611
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007

dbSNP: rs751271
rs751271
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007

dbSNP: rs749910
rs749910
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007

dbSNP: rs3135499
rs3135499
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007

dbSNP: rs2076753
rs2076753
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 GeneticVariation GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789

2007