Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3805322
rs3805322
ADH4 ; LOC100507053
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.800 GeneticVariation GWASDB Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions. 22960999

2012
dbSNP: rs3805322
rs3805322
ADH4 ; LOC100507053
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.800 GeneticVariation GWASCAT Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions. 22960999

2012
dbSNP: rs3805322
rs3805322
ADH4 ; LOC100507053
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.800 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
dbSNP: rs1042365
rs1042365
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs13110176
rs13110176
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs13110764
rs13110764
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs17028615
rs17028615
ADH4 ; LOC100507053
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci. 24166409

2014
dbSNP: rs17028615
rs17028615
ADH4 ; LOC100507053
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci. 24166409

2014
dbSNP: rs17028615
rs17028615
ADH4 ; LOC100507053
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		A 0.700 GeneticVariation GWASDB Genetic determinants influencing human serum metabolome among African Americans. 24625756

2014
dbSNP: rs17028615
rs17028615
ADH4 ; LOC100507053
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci. 24166409

2014
dbSNP: rs17218560
rs17218560
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs17817958
rs17817958
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs1800759
rs1800759
ADH4 ; LOC100507053
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576

2018
dbSNP: rs2602896
rs2602896
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs2851246
rs2851246
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs2851247
rs2851247
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs2851248
rs2851248
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs29001203
rs29001203
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs34936974
rs34936974
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs4699720
rs4699720
ADH4 ; LOC100507053
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs5860563
rs5860563
ADH4 ; LOC100507053
CUI: C0236970
Disease: Alcohol-Induced Disorders
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
dbSNP: rs5860563
rs5860563
ADH4 ; LOC100507053
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.700 GeneticVariation GWASCAT Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. 30940813

2019
dbSNP: rs5860563
rs5860563
ADH4 ; LOC100507053
CUI: C0236664
Disease: Alcohol-Related Disorders
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
dbSNP: rs6532800
rs6532800
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
dbSNP: rs6855482
rs6855482
ADH4 ; LOC100507053
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017