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.
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
323 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.860 1.000 6 2012 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.850 1.000 6 2010 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
223 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.830 1.000 5 2009 2017
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
178 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.800 3 2013 2017
Drinking behavior processes
CUI: C0013124
Disease: Drinking behavior processes
31 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.800 2 2011 2013
Body mass index
CUI: C1305855
Disease: Body mass index
1022 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.800 1 2015 2015
Finding of body mass index
CUI: C0578022
Disease: Finding of body mass index
1022 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.800 1 2015 2015
ALCOHOL SENSITIVITY, ACUTE
CUI: C2674838
Disease: ALCOHOL SENSITIVITY, ACUTE
1 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 14 1983 2010
ESOPHAGEAL CANCER, ALCOHOL-RELATED, SUSCEPTIBILITY TO
1 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 14 1983 2010
HANGOVER, SUSCEPTIBILITY TO (finding)
1 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 14 1983 2010
SUBLINGUAL NITROGLYCERIN, SUSCEPTIBILITY TO POOR RESPONSE TO
1 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 14 1983 2010
Mean corpuscular hemoglobin concentration determination
583 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 2 2010 2017
Erythrocyte Mean Corpuscular Hemoglobin Test
4531 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 1 2017 2017
Finding of Mean Corpuscular Hemoglobin
4531 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 1 2017 2017
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
219 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 1 2010 2010
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
192 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 1 2012 2012
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
435 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 1 2017 2017
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
293 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 1 2018 2018
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
183 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 1 2010 2010
response to alcohol
CUI: C3548532
Disease: response to alcohol
3 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 1 2014 2014
Serum gamma-glutamyl transferase measurement
44 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 1 2010 2010
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
224 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 1 2010 2010
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
2331 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.700 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.040 1.000 4 2010 2015
Squamous cell carcinoma of esophagus
148 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 0.040 1.000 4 2009 2018