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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Coronary heart disease
|
769 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1.000 | 1 | 1998 | 1998 | |||||
Diabetes Mellitus, Non-Insulin-Dependent
|
1598 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.100 | 0.850 | 20 | 1999 | 2017 | |||||
Obesity
|
900 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.100 | 0.846 | 13 | 1999 | 2015 | |||||
Dyslipidemias
|
184 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.050 | 0.800 | 5 | 1999 | 2015 | |||||
Diabetes
|
611 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.030 | 1.000 | 3 | 1999 | 2010 | |||||
Diabetes Mellitus
|
714 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.030 | 1.000 | 3 | 1999 | 2010 | |||||
Impaired glucose tolerance
|
80 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1.000 | 1 | 1999 | 1999 | |||||
Cerebrovascular accident
|
412 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.020 | 0.500 | 2 | 2000 | 2014 | |||||
Atherosclerosis
|
271 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.020 | 1.000 | 2 | 2001 | 2017 | |||||
Hyperinsulinism
|
59 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1 | 2001 | 2001 | ||||||
Hyperlipidemia
|
83 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1 | 2001 | 2001 | ||||||
Obesity, Morbid
|
48 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1.000 | 1 | 2001 | 2001 | |||||
Metabolic Syndrome X
|
477 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.080 | 0.875 | 8 | 2002 | 2015 | |||||
Hyperlipidemia, Familial Combined
|
26 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1.000 | 1 | 2002 | 2002 | |||||
Cardiovascular Diseases
|
382 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.030 | 1.000 | 3 | 2004 | 2013 | |||||
Familial hypercholesterolemia - heterozygous
|
34 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1.000 | 1 | 2004 | 2004 | |||||
Insulin resistance syndrome
|
15 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1.000 | 1 | 2005 | 2005 | |||||
Kidney Diseases
|
131 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1.000 | 1 | 2005 | 2005 | |||||
Hypertriglyceridemia
|
155 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.030 | 1.000 | 3 | 2006 | 2016 | |||||
Carotid Atherosclerosis
|
72 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||
Carotid Stenosis
|
19 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1 | 2007 | 2007 | ||||||
Cerebrovascular Disorders
|
56 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||
Cerebral Infarction
|
123 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.020 | 1.000 | 2 | 2008 | 2014 | |||||
Hypertensive disease
|
871 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.020 | 1.000 | 2 | 2008 | 2015 | |||||
Chronic Kidney Diseases
|
155 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 0.010 | 1.000 | 1 | 2009 | 2009 |