rs1229984, ADH1B

N. diseases: 83
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
0.840 GeneticVariation GWASDB Strong interaction between the effects of alcohol consumption and smoking on oesophageal squamous cell carcinoma among individuals with ADH1B and/or ALDH2 risk alleles. 20833657 2010
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
0.840 GeneticVariation BEFREE ADH1B Arg47His polymorphism is associated with esophageal cancer risk in high-incidence Asian population: evidence from a meta-analysis. 21048924 2010
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
0.840 GeneticVariation GWASCAT Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk. 19698717 2009
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
0.800 GeneticVariation GWASCAT We also observed a genome-wide significant association in non-Hispanic whites between the previously reported SNP rs1229984 in ADH1B and both alcohol consumption phenotypes (OR=0.79, P=2.47 × 10<sup>-20</sup> for drinker status and beta=-0.19, P=1.91 × 10<sup>-35</sup> for drinks/week), which replicated in Hispanic/Latinos (OR=0.72, P=4.35 × 10<sup>-7</sup> and beta=-0.21, P=2.58 × 10<sup>-6</sup>, respectively). 28485404 2017
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
0.800 GeneticVariation GWASCAT A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. 23743675 2013
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
0.800 GeneticVariation GWASDB A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. 23743675 2013
Head and Neck Neoplasms
CUI: C0018671
Disease: Head and Neck Neoplasms
0.800 GeneticVariation GWASCAT A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. 21437268 2011
Head and Neck Neoplasms
CUI: C0018671
Disease: Head and Neck Neoplasms
0.800 GeneticVariation GWASDB A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. 21437268 2011
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
0.750 GeneticVariation BEFREE Our results suggested that ADH1B gene Arg47His variant was associated with the decreased esophageal cancer risk. 27450204 2016
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
0.750 GeneticVariation BEFREE ADH1B rs1229984 polymorphism HRs for HNC and oesophageal cancer death and for alcohol related cancer death were 0.67 (95% CI: 0.42-1.08), and 0.64 (95% CI: 0.40-1.03), respectively. 25770642 2015
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
0.750 GeneticVariation BEFREE The functional polymorphisms ADH1B rs1229984 may contribute to susceptibility to esophageal cancer. 24093763 2014
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
0.750 GeneticVariation BEFREE In conclusion, our findings indicated that ADH1B (rs1229984) was associated with EC independent of alcohol drinking and tobacco smoking status and alcohol drinking interacted with ALDH2 (rs671) on EC susceptibility in this high-risk Chinese population. 22930414 2013
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
0.750 GeneticVariation BEFREE ADH1B Arg47His polymorphism is associated with esophageal cancer risk in high-incidence Asian population: evidence from a meta-analysis. 21048924 2010
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
0.750 GeneticVariation GWASDB Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk. 19698717 2009
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
0.710 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
0.710 GeneticVariation BEFREE To use the rs1229984 variant in the alcohol dehydrogenase 1B gene (ADH1B) as an instrument to investigate the causal role of alcohol in cardiovascular disease. 25011450 2014
Alcohol-Related Disorders
CUI: C0236664
Disease: Alcohol-Related Disorders
0.700 GeneticVariation GWASCAT Genome-wide association studies of alcohol dependence, DSM-IV criterion count and individual criteria. 31090166 2019
Alcohol-Induced Disorders
CUI: C0236970
Disease: Alcohol-Induced Disorders
0.700 GeneticVariation GWASCAT Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. 30940813 2019
Alcohol-Induced Disorders
CUI: C0236970
Disease: Alcohol-Induced Disorders
0.700 GeneticVariation GWASCAT Genome-wide association studies of alcohol dependence, DSM-IV criterion count and individual criteria. 31090166 2019
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
Sodium measurement
CUI: C0337443
Disease: Sodium measurement
0.700 GeneticVariation GWASCAT GWAS for urinary sodium and potassium excretion highlights pathways shared with cardiovascular traits. 31409800 2019
Body mass index
CUI: C1305855
Disease: Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
Alcohol-Related Disorders
CUI: C0236664
Disease: Alcohol-Related Disorders
0.700 GeneticVariation GWASCAT Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. 30940813 2019
Blood urea nitrogen measurement
CUI: C0005845
Disease: Blood urea nitrogen measurement
0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019