| Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|
Crohn Disease
|
0.830 | GeneticVariation | BEFREE | Six single-nucleotide polymorphisms (SNPs) associated with CD were evaluated in these patients: rs2076756, rs2066844, and rs2066845 in NOD2, rs4958847 and rs13361189 in IRGM, and rs2241880 in ATG16L1. | 31714311 | 2019 | |||||
Crohn Disease
|
0.830 | GeneticVariation | BEFREE | The NOD2 single nucleotide polymorphism rs2076756 was associated with younger age at Crohn's disease diagnosis (p = 0.0002). | 25664710 | 2015 | |||||
Crohn Disease
|
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 | |||||
Crohn Disease
|
0.830 | 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 | |||||
Crohn Disease
|
0.830 | GeneticVariation | GWASDB | A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. | 22412388 | 2012 | |||||
Crohn Disease
|
0.830 | GeneticVariation | GWASCAT | A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. | 22412388 | 2012 | |||||
Crohn Disease
|
0.830 | GeneticVariation | GWASDB | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. | 21102463 | 2010 | |||||
Crohn Disease
|
0.830 | GeneticVariation | GWASCAT | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. | 21102463 | 2010 | |||||
Crohn Disease
|
0.830 | GeneticVariation | BEFREE | The NOD2 variants rs2066843 and rs2076756 are novel and common CD susceptibility gene variants. | 21209938 | 2010 | |||||
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 | |||||
Crohn Disease
|
0.830 | GeneticVariation | GWASDB | Systematic association mapping identifies NELL1 as a novel IBD disease gene. | 17684544 | 2007 | |||||
Crohn Disease
|
0.830 | GeneticVariation | GWASCAT | Systematic association mapping identifies NELL1 as a novel IBD disease gene. | 17684544 | 2007 | |||||
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 | |||||
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 |