rs1801177, LPL

N. diseases: 14
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.
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.700 0
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.050 1.000 5 1995 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.040 1.000 4 1995 2016
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.030 1.000 3 1999 2000
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.020 1.000 2 1995 2016
Hyperlipoproteinemia Type I
CUI: C0023817
Disease: Hyperlipoproteinemia Type I
64 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.020 1.000 2 1996 1996
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.010 1.000 1 2018 2018
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.010 1.000 1 2018 2018
Classical Hodgkin's Lymphoma
CUI: C1333064
Disease: Classical Hodgkin's Lymphoma
20 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.010 1.000 1 1995 1995
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.010 1.000 1 2003 2003
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.010 1.000 1 1995 1995
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.010 1 2000 2000
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.010 1.000 1 1995 1995
Peripheral arterial stenosis
CUI: C4025272
Disease: Peripheral arterial stenosis
5 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.010 1.000 1 1995 1995