rs11542041, APOE

N. diseases: 23
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.
Hyperlipoproteinemia Type III
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
24 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.100 1.000 12 1987 2014
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.040 0.750 4 1984 2004
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.030 1.000 3 1998 2000
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.030 1.000 3 1998 2000
Hyperkeratosis lenticularis perstans
CUI: C0263420
Disease: Hyperkeratosis lenticularis perstans
11 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.030 1.000 3 1995 2001
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.030 1.000 3 2004 2007
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2006 2006
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1 2009 2009
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2015 2015
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1 2009 2009
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2005 2005
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2005 2005
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2005 2005
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2015 2015
Endometrial Hyperplasia
CUI: C0014173
Disease: Endometrial Hyperplasia
6 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2015 2015
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1 1993 1993
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2014 2014
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 1988 1988
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2014 2014
Hyperlipoproteinemias
CUI: C0020476
Disease: Hyperlipoproteinemias
7 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 1997 1997
LIPOPROTEIN GLOMERULOPATHY
CUI: C2673196
Disease: LIPOPROTEIN GLOMERULOPATHY
3 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2007 2007
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2015 2015
Polygenic hypercholesterolemia
CUI: C0342880
Disease: Polygenic hypercholesterolemia
3 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 1988 1988