Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6454674
rs6454674
0.020 GeneticVariation BEFREE This study confirms the association between rs6454674 and CD. 21790903

2013

dbSNP: rs6454674
rs6454674
0.020 GeneticVariation BEFREE The interaction between two independent CNR1 variants, ie, the G allele-containing genotypes of rs6454674 (SNP3(G+)), and the T/T genotype of rs806368 (SNP8(T)/T), significantly increased risk for CD in the EA family (P(GEE)=0.015) and EA case-control (P(regression)=0.003) samples. 19052543

2009