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 DUE TO ACTIVATED PROTEIN C RESISTANCE (disorder)
6 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.810 0.667 3 1995 2013
Activated Protein C Resistance
CUI: C0600433
Disease: Activated Protein C Resistance
30 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.800 0.941 17 1995 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.740 0.400 5 1996 2016
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
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
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
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
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
Pulmonary Embolism
CUI: C0034065
Disease: Pulmonary Embolism
16 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.700 1.000 1 2016 2016
Venous Thrombosis
CUI: C0042487
Disease: Venous Thrombosis
218 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.700 1.000 1 2012 2012
BUDD-CHIARI SYNDROME, SUSCEPTIBILITY TO
1 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.700 0
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1
1 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.700 0
STROKE, ISCHEMIC, SUSCEPTIBILITY TO
CUI: C1856857
Disease: STROKE, ISCHEMIC, SUSCEPTIBILITY TO
2 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.700 0
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.100 0.938 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
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
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
Pulmonary Thromboembolisms
CUI: C0524702
Disease: Pulmonary Thromboembolisms
6 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.020 0.500 2 1996 1998
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
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1 2014 2014
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