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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Myocardial Infarction
|
680 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.040 | 1.000 | 4 | 2003 | 2016 | ||||||
Coronary Arteriosclerosis
|
440 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.020 | 0.500 | 2 | 2003 | 2005 | ||||||
Coronary Artery Disease
|
1577 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2004 | 2005 | ||||||
Acute myocardial infarction
|
118 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2004 | 2004 | ||||||
Acute Promyelocytic Leukemia
|
21 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
Angina, Unstable
|
21 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||||
Arteriosclerosis
|
267 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||||
Asthma
|
1536 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
Astrocytoma
|
59 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
Atherosclerosis
|
281 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||||
Chronic Kidney Diseases
|
306 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
Coronary heart disease
|
1178 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||||
Coronary Stenosis
|
20 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||||
Deep Vein Thrombosis
|
93 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
Diabetic Retinopathy
|
213 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1 | 2002 | 2002 | |||||||
Ischemic stroke
|
704 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
Malaria
|
148 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2001 | 2001 | ||||||
Retinoic acid syndrome
|
3 | 0.695 | 0.360 | 17 | 64377836 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2007 | 2007 |