Disease: Nicotine Dependence ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence 		0.020 GeneticVariation disease BEFREE A significant aggregate contribution of rare and common coding variants in CHRNA9 to the risk for ND (SKAT-C: P=0.0012) was detected by applying the combined sum test in MSTCC EAs. 25450229 2015
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence 		0.020 GeneticVariation disease BEFREE We found nominally significant (P<0.05) allelic and genotypic association with smoking initiation of SNP rs2072660 and multilocus haplotypes (P<0.007-0.05) in CHRNB2 and nominal (P<0.05) allelic or genotypic association of SNPs in CHRNA7 (rs1909884), CHRNA9 (rs4861065) and CHRNB3 (rs9298629) with nicotine dependence. 16314871 2006