rs6025, F5

N. diseases: 43
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.
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.900 1.000 16 1997 2019
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.060 1.000 6 1995 2020
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.730 1.000 4 1998 2016
Antithrombin III Deficiency
CUI: C0272375
Disease: Antithrombin III Deficiency
52 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.030 1.000 3 1996 2018
Hereditary Factor V Deficiency
CUI: C0015499
Disease: Hereditary Factor V Deficiency
7 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.700 1.000 3 1994 1994
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.020 1.000 2 2016 2020
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.020 1.000 2 2016 2020
Acquired porencephaly
CUI: C0151860
Disease: Acquired porencephaly
3 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 1998 1998
Antiphospholipid Syndrome
CUI: C0085278
Disease: Antiphospholipid Syndrome
17 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 1996 1996
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
31 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2018 2018
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2016 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.700 1.000 1 2016 2016
Congenital porencephaly
CUI: C0302892
Disease: Congenital porencephaly
3 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 1998 1998
Dysfibrinogenemia
CUI: C1260903
Disease: Dysfibrinogenemia
6 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2000 2000
Eclampsia
CUI: C0013537
Disease: Eclampsia
38 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2012 2012
Endotoxemia
CUI: C0376618
Disease: Endotoxemia
5 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2003 2003
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 1996 1996
HELLP Syndrome
CUI: C0162739
Disease: HELLP Syndrome
10 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 1996 1996
Hemophilia A
CUI: C0019069
Disease: Hemophilia A
295 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2014 2014
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.700 1.000 1 2015 2015
Malnutrition
CUI: C0162429
Disease: Malnutrition
29 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 1995 1995
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2010 2010
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.700 1.000 1 2019 2019
Peripheral Vascular Diseases
CUI: C0085096
Disease: Peripheral Vascular Diseases
18 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 1998 1998
Porencephaly
CUI: C4082173
Disease: Porencephaly
3 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 1998 1998