rs35761398, CNR2

N. diseases: 19
Disease: Crohn Disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
0.010 GeneticVariation BEFREE The CB2-Q63R variant contributes to the risk for pediatric IBD, in particular CD. 27875353 2019