rs11066001, BRAP

N. diseases: 15
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.700 1.000 2 2012 2013
Alcohol-Induced Disorders
CUI: C0236970
Disease: Alcohol-Induced Disorders
180 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.700 1.000 1 2019 2019
Alcohol-Related Disorders
CUI: C0236664
Disease: Alcohol-Related Disorders
180 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.700 1.000 1 2019 2019
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
441 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.700 1.000 1 2019 2019
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.700 1.000 1 2011 2011
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.020 0.500 2 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.020 0.500 2 2009 2011
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.020 0.500 2 2011 2011
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.010 1.000 1 2013 2013
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.010 1 2011 2011
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.010 1.000 1 2013 2013
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.010 1.000 1 2011 2011
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.010 1.000 1 2011 2011
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.010 1.000 1 2013 2013
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.010 1 2011 2011