Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1268
Gene Symbol: CNR1
CNR1
0.530 Biomarker disease BEFREE In this study, we attempt to replicate findings associating CNR1 with CD in African Americans. 21790903 2013
Entrez Id: 1268
Gene Symbol: CNR1
CNR1
0.530 Biomarker disease PSYGENET 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
Entrez Id: 1268
Gene Symbol: CNR1
CNR1
0.530 GeneticVariation disease BEFREE (AAT)n repeat in the cannabinoid receptor gene (CNR1): association with cocaine addiction in an African-Caribbean population. 16314880 2006
Entrez Id: 1268
Gene Symbol: CNR1
CNR1
0.530 Biomarker disease CTD_human (AAT)n repeat in the cannabinoid receptor gene (CNR1): association with cocaine addiction in an African-Caribbean population. 16314880 2006
Entrez Id: 1268
Gene Symbol: CNR1
CNR1
0.530 Biomarker disease PSYGENET (AAT)n repeat in the cannabinoid receptor gene (CNR1): association with cocaine addiction in an African-Caribbean population. 16314880 2006
Entrez Id: 1268
Gene Symbol: CNR1
CNR1
0.530 Biomarker disease PSYGENET In this study, we attempt to replicate findings associating CNR1 with CD in African Americans. 21790903 2013
Entrez Id: 1268
Gene Symbol: CNR1
CNR1
0.530 GeneticVariation disease 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
Entrez Id: 1268
Gene Symbol: CNR1
CNR1
0.530 Biomarker disease CTD_human Role of cannabinoid type 1 receptors in locomotor activity and striatal signaling in response to psychostimulants. 17596442 2007
Entrez Id: 1268
Gene Symbol: CNR1
CNR1
0.530 Biomarker disease CTD_human 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