Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.060 0.833 6 2006 2018
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation 		0.040 0.750 4 2006 2015
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.030 1.000 3 2014 2019
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		0.030 1.000 3 2005 2009
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.030 1.000 3 2003 2012
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.030 0.667 3 2003 2014
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity 		0.020 1.000 2 2014 2016
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C3495426
Disease: Homocysteinemia
Homocysteinemia 		0.020 1.000 2 1997 2009
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.020 0.500 2 2007 2017
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		0.020 0.500 2 2013 2015
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder 		0.020 1.000 2 2005 2009
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia 		0.020 1.000 2 2007 2019
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.020 1.000 2 2005 2014
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C3160845
Disease: PAI-1 4G/5G polymorphism
PAI-1 4G/5G polymorphism 		0.020 < 0.001 2 2011 2014
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.020 0.500 2 2014 2018
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.010 1.000 1 2003 2003
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C4552766
Disease: Miscarriage
Miscarriage 		0.010 1.000 1 2013 2013
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0795687
Disease: Cerebral arterial thrombosis
Cerebral arterial thrombosis 		0.010 1.000 1 2007 2007
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0019061
Disease: Hemolytic-Uremic Syndrome
Hemolytic-Uremic Syndrome 		0.010 1.000 1 2001 2001
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome 		0.010 1.000 1 2006 2006
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.010 1.000 1 2018 2018
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 1999 1999
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs763351020
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2003 2003