Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2501432
rs2501432
CNR2
CUI: C0003864
Disease: Arthritis
Arthritis 		0.010 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