Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.900 1.000 19 2004 2019
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
Digestive System Diseases; Neoplasms 0.840 1.000 6 2009 2016
dbSNP: rs1789891
rs1789891
1.000 0.080 4 99329262 intron variant C/A snv 0.13
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.820 1.000 4 2012 2019
dbSNP: rs1042026
rs1042026
1.000 0.080 4 99307309 3 prime UTR variant T/C snv 0.24
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
Digestive System Diseases; Neoplasms 0.800 1.000 2 2010 2012
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
Behavior and Behavior Mechanisms 0.800 1.000 2 2013 2017
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0018671
Disease: Head and Neck Neoplasms
Head and Neck Neoplasms
Neoplasms 0.800 1.000 1 2011 2011
dbSNP: rs1229984
rs1229984
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
Digestive System Diseases; Neoplasms 0.750 1.000 6 2009 2016
dbSNP: rs2066702
rs2066702
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
Chemically-Induced Disorders; Mental Disorders 0.720 1.000 4 2014 2019
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.710 1.000 2 2014 2019
dbSNP: rs1614972
rs1614972
0.925 0.160 4 99336998 intron variant C/T snv 0.38
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.710 1.000 2 2013 2014
dbSNP: rs2173201
rs2173201
1.000 0.080 4 99329813 intron variant C/A snv 0.30
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.710 1.000 2 2014 2014
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders
Chemically-Induced Disorders; Mental Disorders 0.700 1.000 4 2013 2019
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders
Chemically-Induced Disorders 0.700 1.000 4 2013 2019
dbSNP: rs1229984
rs1229984
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: rs1789891
rs1789891
1.000 0.080 4 99329262 intron variant C/A snv 0.13
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders
Chemically-Induced Disorders; Mental Disorders 0.700 1.000 2 2012 2017
dbSNP: rs1789891
rs1789891
1.000 0.080 4 99329262 intron variant C/A snv 0.13
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders
Chemically-Induced Disorders 0.700 1.000 2 2012 2017
dbSNP: rs2066702
rs2066702
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
Chemically-Induced Disorders 0.700 1.000 2 2014 2019
dbSNP: rs2066702
rs2066702
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
Chemically-Induced Disorders; Mental Disorders 0.700 1.000 2 2014 2019
dbSNP: rs1154433
rs1154433
1.000 0.080 4 99332551 intron variant A/G;T snv
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs1154433
rs1154433
1.000 0.080 4 99332551 intron variant A/G;T snv
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders
Chemically-Induced Disorders 0.700 1.000 1 2019 2019
dbSNP: rs1154433
rs1154433
1.000 0.080 4 99332551 intron variant A/G;T snv
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders
Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0337443
Disease: Sodium measurement
Sodium measurement
0.700 1.000 1 2019 2019
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
Primary malignant neoplasm of lateral wall of oropharynx
0.700 1.000 1 2016 2016
dbSNP: rs1229984
rs1229984
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
0.700 1.000 1 2019 2019