rs3135506, APOA5

N. diseases: 26
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.800 1.000 4 2009 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.700 1.000 3 2018 2019
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.700 1.000 2 2018 2019
HYPERTRIGLYCERIDEMIA, SUSCEPTIBILITY TO
CUI: C4016963
Disease: HYPERTRIGLYCERIDEMIA, SUSCEPTIBILITY TO
3 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.700 0
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.070 1.000 7 2007 2016
Obesity
CUI: C0028754
Disease: Obesity
1111 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.060 1.000 6 2007 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.050 0.800 5 2007 2018
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.050 1.000 5 2007 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.030 1.000 3 2005 2013
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.030 1.000 3 2008 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.030 1.000 3 2014 2018
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.030 1.000 3 2008 2017
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.020 1.000 2 2007 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.020 1.000 2 2008 2010
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.020 1.000 2 2007 2009
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.020 1.000 2 2008 2014
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.020 0.500 2 2006 2007
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.020 1.000 2 2008 2015
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.010 1.000 1 2004 2004
Atherogenic dyslipidaemia
CUI: C4524040
Disease: Atherogenic dyslipidaemia
9 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.010 1.000 1 2015 2015
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.010 1.000 1 2004 2004
Avascular Necrosis of Femur Head
CUI: C0410480
Disease: Avascular Necrosis of Femur Head
20 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.010 1.000 1 2014 2014
Diabetic dyslipidaemia
CUI: C3160761
Disease: Diabetic dyslipidaemia
11 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.010 1.000 1 2008 2008
Hyperlipoproteinemia Type I
CUI: C0023817
Disease: Hyperlipoproteinemia Type I
64 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.010 1.000 1 2008 2008
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.010 1.000 1 2016 2016