Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12481514
rs12481514
ADRA1D
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		A 0.700 GeneticVariation GWASCAT LRRK2 but not ATG16L1 is associated with Paneth cell defect in Japanese Crohn's disease patients. 28352666

2017