Disease: Crohn Disease ×
Source: GWASCAT ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2076756
rs2076756
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
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
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
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
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
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
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease 		0.830 GeneticVariation GWASCAT Systematic association mapping identifies NELL1 as a novel IBD disease gene. 17684544 2007
dbSNP: rs2076756
rs2076756
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
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