rs11066280, HECTD4

N. diseases: 18
Source: CURATED ×
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
469 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.800 1.000 3 2012 2013
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
118 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.800 1.000 2 2010 2011
Drinking behavior processes
CUI: C0013124
Disease: Drinking behavior processes
31 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.800 1.000 1 2013 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
233 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.710 1.000 1 2014 2015
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 3 2011 2015
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 3 2011 2015
Alanine aminotransferase measurement
CUI: C0201836
Disease: Alanine aminotransferase measurement
77 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 2 2011 2019
Serum Alanine Aminotransferase Measurement
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
77 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 2 2011 2019
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
535 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2013 2013
Aspartate aminotransferase measurement
CUI: C0201899
Disease: Aspartate aminotransferase measurement
76 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2019 2019
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2011 2011
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2017 2017
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1103 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2013 2013
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
48 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2011 2011
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
124 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2014 2014
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2011 2011
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2016 2016
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2018 2018