Disease: Crohn Disease ×
Source: GWASDB ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2066847
rs2066847
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease 		T 0.890 GeneticVariation GWASDB Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
dbSNP: rs2066847
rs2066847
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease 		0.890 GeneticVariation GWASDB Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. 20570966 2010
dbSNP: rs2066847
rs2066847
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease 		C 0.890 GeneticVariation GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394 2008
dbSNP: rs2066847
rs2066847
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease 		0.890 GeneticVariation GWASDB Systematic association mapping identifies NELL1 as a novel IBD disease gene. 17684544 2007