rs35761398, CNR2

N. diseases: 19
Disease: Celiac Disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
0.020 GeneticVariation BEFREE In humans, the nonsynonymous mutation Q63R, the most common variant of the CB2 receptor, has been found to be associated with multiple diseases, including idiopathic arthritis, obesity, and celiac diseases. 29694791 2018
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
0.020 GeneticVariation BEFREE The Q63R variant, increasing more than six-fold the risk for CD susceptibility, might eventually represent a novel molecular biomarker for CD risk stratification. 22465144 2012