Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2066847
rs2066847
CUI: C0010346
Disease: Crohn 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
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.890 GeneticVariation GWASDB Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. 20570966

2010

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

2007