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.
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
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1 2014 2014
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
Miscarriage
CUI: C4552766
Disease: Miscarriage
56 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1 2017 2017
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
Protein S Deficiency
CUI: C0242666
Disease: Protein S Deficiency
14 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2011 2011
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
Retinopathy of Prematurity
CUI: C0035344
Disease: Retinopathy of Prematurity
16 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2016 2016
Severe hereditary factor VIII deficiency disease
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
15 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2014 2014
Severe Sepsis
CUI: C1719672
Disease: Severe Sepsis
29 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2003 2003
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
CUI: C2676744
Disease: 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
CUI: C3280670
Disease: 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