rs671, ALDH2

N. diseases: 116
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
ESOPHAGEAL CANCER, ALCOHOL-RELATED, SUSCEPTIBILITY TO
CUI: C3149226
Disease: ESOPHAGEAL CANCER, ALCOHOL-RELATED, SUSCEPTIBILITY TO
1 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.700 0
HANGOVER, SUSCEPTIBILITY TO (finding)
CUI: C2608086
Disease: HANGOVER, SUSCEPTIBILITY TO (finding)
1 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.700 0
SUBLINGUAL NITROGLYCERIN, SUSCEPTIBILITY TO POOR RESPONSE TO
CUI: C2676227
Disease: SUBLINGUAL NITROGLYCERIN, SUSCEPTIBILITY TO POOR RESPONSE TO
1 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.700 0
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.880 1.000 10 2001 2019
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.780 1.000 10 2001 2019
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.080 1.000 8 2001 2019
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.020 1.000 2 2002 2015
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
441 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.900 1.000 11 2005 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.080 1.000 8 2005 2016
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.080 1.000 8 2005 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.050 1.000 5 2006 2019
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.010 1.000 1 2006 2006
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.010 1.000 1 2006 2006
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.070 0.857 7 2007 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.040 1.000 4 2007 2014
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.090 1.000 9 2009 2019
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.010 1.000 1 2009 2009
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.010 1.000 1 2009 2009
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.900 1.000 11 2010 2020
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.100 1.000 10 2010 2018
Flushing
CUI: C0016382
Disease: Flushing
9 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.070 1.000 7 2010 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.060 1.000 6 2010 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.040 1.000 4 2010 2019
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.700 1.000 2 2010 2017
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.010 1.000 1 2010 2010