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.
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
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1 2009 2009
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
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 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
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