Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1042026
rs1042026
ADH1B
1.000 0.080 4 99307309 3 prime UTR variant T/C snv 0.24
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.800 1.000 2 2010 2012
dbSNP: rs17033
rs17033
ADH1B
0.925 0.080 4 99307788 3 prime UTR variant T/C snv 9.6E-02
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.700 1.000 1 2012 2012
dbSNP: rs2066702
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		0.700 1.000 2 2014 2019
dbSNP: rs2066702
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		0.700 1.000 2 2014 2019
dbSNP: rs2066702
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.720 1.000 2 2014 2019
dbSNP: rs1789882
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		0.700 1.000 1 2014 2014
dbSNP: rs1789882
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		0.700 1.000 1 2014 2014
dbSNP: rs1789882
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.700 1.000 1 2014 2014
dbSNP: rs1789882
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs1693457
rs1693457
ADH1B
1.000 0.080 4 99315605 non coding transcript exon variant C/T snv 0.81
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.700 1.000 1 2014 2014
dbSNP: rs1693457
rs1693457
ADH1B
1.000 0.080 4 99315605 non coding transcript exon variant C/T snv 0.81
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		0.700 1.000 1 2014 2014
dbSNP: rs1693457
rs1693457
ADH1B
1.000 0.080 4 99315605 non coding transcript exon variant C/T snv 0.81
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		0.700 1.000 1 2014 2014
dbSNP: rs2075633
rs2075633
ADH1B
1.000 0.080 4 99317841 non coding transcript exon variant T/C snv 0.24
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.700 1.000 1 2019 2019
dbSNP: rs2075633
rs2075633
ADH1B
1.000 0.080 4 99317841 non coding transcript exon variant T/C snv 0.24
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		0.700 1.000 1 2019 2019
dbSNP: rs2075633
rs2075633
ADH1B
1.000 0.080 4 99317841 non coding transcript exon variant T/C snv 0.24
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		0.700 1.000 1 2019 2019
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.900 1.000 4 2004 2019
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		0.700 1.000 4 2013 2019
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		0.700 1.000 4 2013 2019
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.840 1.000 2 2009 2016
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.800 1.000 2 2013 2017
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2017 2019
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.750 1.000 1 2009 2016
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C3165521
Disease: Primary malignant neoplasm of lateral wall of oropharynx
Primary malignant neoplasm of lateral wall of oropharynx 		0.700 1.000 1 2016 2016
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0153368
Disease: Malignant neoplasm of floor of mouth
Malignant neoplasm of floor of mouth 		0.700 1.000 1 2016 2016
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0153390
Disease: Malignant neoplasm of posterior wall of oropharynx
Malignant neoplasm of posterior wall of oropharynx 		0.700 1.000 1 2016 2016