rs7412, APOE

N. diseases: 47
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.
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 1 2017 2017
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2018 2018
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.030 1.000 3 2014 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.720 1.000 5 2011 2019
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2010 2010
AURAL ATRESIA, CONGENITAL
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
29 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2016 2016
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 3 2018 2018
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.710 1.000 2 2016 2019
Cerebral Vasospasm
CUI: C0265110
Disease: Cerebral Vasospasm
3 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2018 2018
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2015 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.730 1.000 6 2012 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.720 1.000 3 2017 2019
Dementia
CUI: C0497327
Disease: Dementia
176 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1 2010 2010
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2019 2019
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2011 2011
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2015 2015
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2019 2019
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 1 2019 2019
Hepatitis E
CUI: C0085293
Disease: Hepatitis E
2 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2018 2018
Hepatolenticular Degeneration
CUI: C0019202
Disease: Hepatolenticular Degeneration
349 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2018 2018
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 4 2017 2019
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2014 2014
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2018 2018
Hyperlipoproteinemia Type III
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
24 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 0
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2014 2014