rs763351020, SERPINE1

N. diseases: 35
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.
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.060 0.833 6 2006 2018
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.040 0.750 4 2006 2015
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.030 1.000 3 2014 2019
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.030 0.667 3 2003 2014
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.030 1.000 3 2005 2009
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.030 1.000 3 2003 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.020 0.500 2 2007 2017
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.020 1.000 2 2005 2014
Homocysteinemia
CUI: C3495426
Disease: Homocysteinemia
6 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.020 1.000 2 1997 2009
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.020 1.000 2 2007 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.020 0.500 2 2014 2018
Lupus anticoagulant disorder
CUI: C0311370
Disease: Lupus anticoagulant disorder
14 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.020 1.000 2 2005 2009
Obesity
CUI: C0028754
Disease: Obesity
1111 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.020 1.000 2 2014 2016
PAI-1 4G/5G polymorphism
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
3 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.020 2 2011 2014
Retinal Vein Occlusion
CUI: C0035328
Disease: Retinal Vein Occlusion
15 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.020 0.500 2 2013 2015
Activated Protein C Resistance
CUI: C0600433
Disease: Activated Protein C Resistance
30 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.010 1.000 1 2010 2010
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
176 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.010 1.000 1 2006 2006
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.010 1.000 1 2003 2003
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.010 1.000 1 2013 2013
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.010 1.000 1 2013 2013
Cerebral arterial thrombosis
CUI: C0795687
Disease: Cerebral arterial thrombosis
9 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.010 1.000 1 2007 2007
Cerebral Thrombosis
CUI: C0079102
Disease: Cerebral Thrombosis
7 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.010 1.000 1 2007 2007
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.010 1.000 1 2018 2018
Colitis, Ischemic
CUI: C0162529
Disease: Colitis, Ischemic
3 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.010 1.000 1 2015 2015
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 0.010 1 2011 2011