rs1799963, F2

N. diseases: 25
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.
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.810 1.000 6 2001 2016
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.730 1.000 8 2012 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.720 1.000 3 2015 2016
THROMBOPHILIA DUE TO THROMBIN DEFECT
CUI: C3160733
Disease: THROMBOPHILIA DUE TO THROMBIN DEFECT
2 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.700 1.000 14 1986 2013
Inherited Factor II deficiency
CUI: C0020640
Disease: Inherited Factor II deficiency
13 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.700 1.000 2 1998 2009
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.700 1.000 1 2016 2016
Pulmonary Embolism
CUI: C0034065
Disease: Pulmonary Embolism
16 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.700 1.000 1 2016 2016
Hereditary factor II deficiency disease
CUI: C0272317
Disease: Hereditary factor II deficiency disease
14 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.700 0
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2
CUI: C3280672
Disease: PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2
1 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.700 0
STROKE, ISCHEMIC, SUSCEPTIBILITY TO
CUI: C1856857
Disease: STROKE, ISCHEMIC, SUSCEPTIBILITY TO
2 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.700 0
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.040 1.000 4 2012 2020
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1 2014 2014
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1.000 1 2016 2016
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1.000 1 2016 2016
Fetal Growth Retardation
CUI: C0015934
Disease: Fetal Growth Retardation
21 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1.000 1 2017 2017
Hemophilia A
CUI: C0019069
Disease: Hemophilia A
295 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1.000 1 2014 2014
Juvenile Myoclonic Epilepsy
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
46 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1 2015 2015
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1 2011 2011
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1 2014 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1.000 1 2020 2020
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1.000 1 2017 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1.000 1 2020 2020
Protein S Deficiency
CUI: C0242666
Disease: Protein S Deficiency
14 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1.000 1 2011 2011
Retinopathy of Prematurity
CUI: C0035344
Disease: Retinopathy of Prematurity
16 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1.000 1 2016 2016
Severe hereditary factor VIII deficiency disease
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
15 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.010 1.000 1 2014 2014