rs1188383936, F2

N. diseases: 102
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.
Factor V Leiden mutation
CUI: C0584960
Disease: 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
CUI: C0398623
Disease: 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
CUI: C1861172
Disease: 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
CUI: C0598608
Disease: 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
CUI: C0149871
Disease: 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
CUI: C0948008
Disease: 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
CUI: C0600433
Disease: 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
CUI: C0002895
Disease: 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
CUI: C0038454
Disease: 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
CUI: C4552766
Disease: 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
CUI: C1956346
Disease: 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
CUI: C0242666
Disease: 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
CUI: C2584409
Disease: 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
CUI: C0004943
Disease: 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
CUI: C0007222
Disease: 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
CUI: C0015934
Disease: 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
CUI: C0027051
Disease: 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
CUI: C1260403
Disease: 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
CUI: C0035328
Disease: 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
CUI: C2584620
Disease: 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
CUI: C0272375
Disease: 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
CUI: C0856761
Disease: 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
CUI: C0007785
Disease: 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
CUI: C0007820
Disease: 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
CUI: C0002875
Disease: 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