rs118204057, LPL

N. diseases: 16
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 I
CUI: C0023817
Disease: Hyperlipoproteinemia Type I
64 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.860 0.963 27 1990 2012
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.700 0
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.030 1.000 3 1998 2020
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.030 1.000 3 1997 2002
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.020 0.500 2 1998 1998
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
80 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.020 1.000 2 1996 2020
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 2008 2008
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 2008 2008
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 1999 1999
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 2008 2008
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 2003 2003
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 1998 1998
Hyperkeratosis lenticularis perstans
CUI: C0263420
Disease: Hyperkeratosis lenticularis perstans
11 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 1995 1995
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 1998 1998
Nuchal bleb, familial
CUI: C0948242
Disease: Nuchal bleb, familial
9 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 1996 1996
Retrosternal pain
CUI: C0151826
Disease: Retrosternal pain
7 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 1998 1998