rs5882, CETP

N. diseases: 32
Source: BEFREE ×
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.
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
968 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.070 1.000 7 2007 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
769 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.070 1.000 7 1998 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1022 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.060 1.000 6 2009 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.040 1.000 4 2009 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
382 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.030 1.000 3 2007 2016
Dementia
CUI: C0497327
Disease: Dementia
165 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.030 1.000 3 2010 2017
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.030 1.000 3 2010 2017
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.020 0.500 2 2012 2015
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
266 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.020 1.000 2 1999 2012
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
271 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.020 1.000 2 1999 2012
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
72 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.020 0.500 2 2012 2014
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
25 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.020 1.000 2 2009 2018
Diabetes Mellitus, Non-Insulin-Dependent
1598 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.020 1.000 2 2018 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
871 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.020 1.000 2 2018 2018
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
223 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.020 1.000 2 2012 2015
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
90 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.020 1.000 2 2012 2015
Obesity
CUI: C0028754
Disease: Obesity
900 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.020 1.000 2 2010 2011
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.010 1 2008 2008
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
390 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.010 1.000 1 2017 2017
Anxiety
CUI: C0003467
Disease: Anxiety
118 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.010 1.000 1 2017 2017
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
144 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.010 1.000 1 2017 2017
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
155 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.010 1.000 1 2009 2009
Coronary Stenosis
CUI: C0242231
Disease: Coronary Stenosis
20 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.010 1.000 1 2012 2012
Endometriosis
CUI: C0014175
Disease: Endometriosis
207 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.010 1.000 1 2013 2013
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
133 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.010 1.000 1 2009 2009