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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cardiovascular Abnormalities
|
12 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||
Peripheral Arterial Diseases
|
128 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||
Acquired Immunodeficiency Syndrome
|
42 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||
Acute Chest Syndrome
|
135 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||
Acute Coronary Syndrome
|
139 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||
Carcinogenesis
|
355 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1 | 2005 | 2005 | |||||
Cerebrovascular Disorders
|
56 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||
Hepatocarcinogenesis
|
24 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||
Liver carcinoma
|
942 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1 | 2005 | 2005 | |||||
Neoplasm Metastasis
|
327 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1 | 2005 | 2005 | |||||
Neoplasms
|
1644 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1 | 2005 | 2005 | |||||
Anthracosis
|
37 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2006 | 2006 | ||||
Crohn Disease
|
1147 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||
Stenosis of intestine
|
3 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||
Tropical Spastic Paraparesis
|
4 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||
Carotid Atherosclerosis
|
79 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1 | 2009 | 2009 | |||||
Hyperlipidemia
|
83 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1 | 2009 | 2009 | |||||
Asthma
|
1536 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.020 | 1.000 | 2 | 2006 | 2011 | ||||
Chronic kidney disease stage 5
|
194 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.020 | 1.000 | 2 | 2003 | 2011 | ||||
Coronary Arteriosclerosis
|
440 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.020 | 1.000 | 2 | 2008 | 2012 | ||||
Coronary heart disease
|
1178 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.020 | 1.000 | 2 | 2008 | 2012 | ||||
Acute myocardial infarction
|
118 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
Geographic Atrophy
|
81 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
Multiple Sclerosis
|
1022 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
Parkinson Disease
|
990 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 0.010 | 1.000 | 1 | 2012 | 2012 |