Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs55828312
rs55828312
Entrez Id: 1142
Gene Symbol: CHRNB3
CHRNB3
CUI: C0037369
Disease:
Smoking
G 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence. 26440539 2015
dbSNP: rs13280604
rs13280604
Entrez Id: 1142;105379396
Gene Symbol: CHRNB3;LOC105379396
CHRNB3;LOC105379396
CUI: C1519383
Disease:
Smoking Behaviors
0.700 GeneticVariation GWASDB Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. 20418888 2010
dbSNP: rs1530848
rs1530848
Entrez Id: 1142;105379396
Gene Symbol: CHRNB3;LOC105379396
CHRNB3;LOC105379396
CUI: C1519383
Disease:
Smoking Behaviors
0.700 GeneticVariation GWASDB Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. 20418888 2010
dbSNP: rs16891561
rs16891561
Entrez Id: 1142
Gene Symbol: CHRNB3
CHRNB3
CUI: C1519383
Disease:
Smoking Behaviors
0.700 GeneticVariation GWASDB Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. 20418888 2010
dbSNP: rs6474414
rs6474414
Entrez Id: 1142
Gene Symbol: CHRNB3
CHRNB3
CUI: C1519383
Disease:
Smoking Behaviors
0.700 GeneticVariation GWASDB Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. 20418888 2010
dbSNP: rs6474415
rs6474415
Entrez Id: 1142
Gene Symbol: CHRNB3
CHRNB3
CUI: C1519383
Disease:
Smoking Behaviors
0.700 GeneticVariation GWASDB Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. 20418888 2010
dbSNP: rs6997909
rs6997909
Entrez Id: 1142;105379396
Gene Symbol: CHRNB3;LOC105379396
CHRNB3;LOC105379396
CUI: C1519383
Disease:
Smoking Behaviors
0.700 GeneticVariation GWASDB Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. 20418888 2010
dbSNP: rs7004381
rs7004381
Entrez Id: 1142;105379396
Gene Symbol: CHRNB3;LOC105379396
CHRNB3;LOC105379396
CUI: C1519383
Disease:
Smoking Behaviors
0.700 GeneticVariation GWASDB Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. 20418888 2010
dbSNP: rs13280604
rs13280604
Entrez Id: 1142;105379396
Gene Symbol: CHRNB3;LOC105379396
CHRNB3;LOC105379396
CUI: C0028043
Disease:
Nicotine Dependence
0.010 GeneticVariation BEFREE Finally, our meta-analysis of samples with Asian and European origins for five SNPs in CHRNB3 showed significant associations with ND, with p-values ranging from 6.86 × 10<sup>-14</sup> for rs13280604 to 6.50 × 10<sup>-8</sup> for rs4950<sup>.</sup> This represents the first study showing that CHRNB3/A6 are highly associated with ND in a large Chinese Han sample. 28851948 2017
dbSNP: rs13280604
rs13280604
Entrez Id: 1142;105379396
Gene Symbol: CHRNB3;LOC105379396
CHRNB3;LOC105379396
CUI: C0006868
Disease:
Cannabis Abuse
0.010 GeneticVariation BEFREE Rs16969968 in CHRNA5 (and its proxy, rs1051730 in CHRNA3) and rs1451240, a proxy for rs13280604 in CHRNB3, were associated with CPD after Bonferroni correction (p<0.006). rs1451240 was also associated with DSM-IV cannabis abuse/dependence. 25770649 2015
dbSNP: rs13280604
rs13280604
Entrez Id: 1142;105379396
Gene Symbol: CHRNB3;LOC105379396
CHRNB3;LOC105379396
CUI: C0279626
Disease:
Squamous cell carcinoma of esophagus
0.010 GeneticVariation BEFREE We studied the association of the CHRNB3-A6 variant rs13280604 in relation to esophageal squamous cell carcinoma (ESCC) in Chinese populations. 25823894 2015
dbSNP: rs13280604
rs13280604
Entrez Id: 1142;105379396
Gene Symbol: CHRNB3;LOC105379396
CHRNB3;LOC105379396
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE A logistic regression model was used to evaluate the associations of rs13280604 with cancer risk. 25823894 2015
dbSNP: rs13280604
rs13280604
Entrez Id: 1142;105379396
Gene Symbol: CHRNB3;LOC105379396
CHRNB3;LOC105379396
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE A logistic regression model was used to evaluate the associations of rs13280604 with cancer risk. 25823894 2015
dbSNP: rs149775276
rs149775276
Entrez Id: 1142
Gene Symbol: CHRNB3
CHRNB3
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic
0.010 GeneticVariation BEFREE Additionally, one variant (rs149775276; H329Y) shows association with both cocaine dependence symptoms (P = 7.4 × 10(-5), β = 2.04) and alcohol dependence symptoms (P = 2.6 × 10(-4), β = 2.04). 24057674 2014
dbSNP: rs149775276
rs149775276
Entrez Id: 1142
Gene Symbol: CHRNB3
CHRNB3
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic
0.010 GeneticVariation BEFREE Additionally, one variant (rs149775276; H329Y) shows association with both cocaine dependence symptoms (P = 7.4 × 10(-5), β = 2.04) and alcohol dependence symptoms (P = 2.6 × 10(-4), β = 2.04). 24057674 2014
dbSNP: rs149775276
rs149775276
Entrez Id: 1142
Gene Symbol: CHRNB3
CHRNB3
CUI: C0600427
Disease:
Cocaine Dependence
0.010 GeneticVariation BEFREE Additionally, one variant (rs149775276; H329Y) shows association with both cocaine dependence symptoms (P = 7.4 × 10(-5), β = 2.04) and alcohol dependence symptoms (P = 2.6 × 10(-4), β = 2.04). 24057674 2014
dbSNP: rs149775276
rs149775276
Entrez Id: 1142
Gene Symbol: CHRNB3
CHRNB3
CUI: C0600427
Disease:
Cocaine Dependence
0.010 GeneticVariation BEFREE Additionally, one variant (rs149775276; H329Y) shows association with both cocaine dependence symptoms (P = 7.4 × 10(-5), β = 2.04) and alcohol dependence symptoms (P = 2.6 × 10(-4), β = 2.04). 24057674 2014
dbSNP: rs4952
rs4952
Entrez Id: 1142
Gene Symbol: CHRNB3
CHRNB3
CUI: C0028043
Disease:
Nicotine Dependence
0.010 GeneticVariation BEFREE Another SNP in the region, rs4952, remains modestly associated with nicotine dependence in the combined data after conditioning on rs13273442. 24401102 2014
dbSNP: rs13280604
rs13280604
Entrez Id: 1142;105379396
Gene Symbol: CHRNB3;LOC105379396
CHRNB3;LOC105379396
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
0.010 GeneticVariation BEFREE To examine the association of single nucleotide polymorphisms (SNPs) of the CHRNB3 (rs13280604) and CHRNA6 (rs892413) nicotinic acetylcholine receptor (nAChR) genes and symptoms of attention deficit hyperactivity disorder (ADHD) in predicting smoking patterns from early adolescence to adulthood. 23899432 2013
dbSNP: rs4952
rs4952
Entrez Id: 1142
Gene Symbol: CHRNB3
CHRNB3
CUI: C0005586
Disease:
Bipolar Disorder
0.010 GeneticVariation BEFREE In the investigation of pleiotropic effects of these SNPs on bipolar disorder, two highly correlated synonymous SNPs in CHRNB3, rs4952 and rs4953, were significantly associated with bipolar disorder (odds ratio 1.7, 95% confidence interval: 1.2-2.4, P=0.001). 21191315 2011
dbSNP: rs4953
rs4953
Entrez Id: 1142
Gene Symbol: CHRNB3
CHRNB3
CUI: C0005586
Disease:
Bipolar Disorder
0.010 GeneticVariation BEFREE In the investigation of pleiotropic effects of these SNPs on bipolar disorder, two highly correlated synonymous SNPs in CHRNB3, rs4952 and rs4953, were significantly associated with bipolar disorder (odds ratio 1.7, 95% confidence interval: 1.2-2.4, P=0.001). 21191315 2011