Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2066843
rs2066843
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.710 GeneticVariation BEFREE The NOD2 variants rs2066843 and rs2076756 are novel and common CD susceptibility gene variants. 21209938

2010
dbSNP: rs2066843
rs2066843
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.710 GeneticVariation GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223

2006