Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10883365
rs10883365
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
G 0.830 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007

dbSNP: rs10883365
rs10883365
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.830 GeneticVariation GWASCAT Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. 17554261

2007