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.
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
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
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
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
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
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
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
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
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2016 2016
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1 2014 2014
Osteopenia
CUI: C0029453
Disease: Osteopenia
61 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2010 2010
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2010 2010
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2015 2015
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1 2010 2010
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.020 0.500 2 2012 2015
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.020 1.000 2 2009 2019
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
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