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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Factor V Leiden mutation
|
46 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.100 | 0.912 | 34 | 1998 | 2019 | |||||
Thrombophilia
|
43 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.100 | 0.947 | 19 | 1999 | 2018 | |||||
Venous Thromboembolism
|
408 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.100 | 0.895 | 19 | 2000 | 2015 | |||||
Hyperhomocysteinemia
|
45 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.100 | 1.000 | 13 | 1999 | 2016 | |||||
Deep Vein Thrombosis
|
93 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.090 | 1.000 | 9 | 1999 | 2015 | |||||
Ischemic stroke
|
704 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.090 | 0.778 | 9 | 2001 | 2013 | |||||
Activated Protein C Resistance
|
30 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.060 | 0.833 | 6 | 2002 | 2016 | |||||
Anemia, Sickle Cell
|
138 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.050 | 1.000 | 5 | 1998 | 2013 | |||||
Cerebrovascular accident
|
591 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.050 | 1.000 | 5 | 1999 | 2016 | |||||
Miscarriage
|
56 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.050 | 1.000 | 5 | 2000 | 2016 | |||||
Coronary Artery Disease
|
1577 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.040 | 0.750 | 4 | 2000 | 2009 | |||||
Protein S Deficiency
|
14 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.040 | 1.000 | 4 | 2001 | 2016 | |||||
Prothrombin G20210A mutation
|
9 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.040 | 0.750 | 4 | 2001 | 2008 | |||||
Behcet Syndrome
|
243 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.030 | 0.667 | 3 | 2000 | 2013 | |||||
Cardiovascular Diseases
|
711 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.030 | 1.000 | 3 | 2011 | 2019 | |||||
Fetal Growth Retardation
|
21 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.030 | 1.000 | 3 | 2002 | 2009 | |||||
Myocardial Infarction
|
680 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.030 | 1.000 | 3 | 1999 | 2008 | |||||
prothrombin gene mutation
|
5 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.030 | 0.667 | 3 | 2003 | 2012 | |||||
Retinal Vein Occlusion
|
15 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.030 | 1.000 | 3 | 2003 | 2017 | |||||
Thrombophilia, hereditary
|
9 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.030 | 1.000 | 3 | 2001 | 2013 | |||||
Antithrombin III Deficiency
|
52 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.020 | 1.000 | 2 | 2000 | 2005 | |||||
Budd-Chiari Syndrome
|
4 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.020 | 1.000 | 2 | 2004 | 2016 | |||||
Cerebral Infarction
|
123 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.020 | 1.000 | 2 | 2000 | 2009 | |||||
Cerebrovascular Disorders
|
56 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.020 | 1.000 | 2 | 2000 | 2011 | |||||
Cooley's anemia
|
19 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 0.020 | 1.000 | 2 | 2008 | 2009 |