rs1799963, F2

N. diseases: 18
Source: BEFREE ×
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
412 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.810 1.000 1 2001 2016
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
106 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.730 1.000 3 2012 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
586 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.720 1.000 2 2015 2016
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
2145 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
382 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
19 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
36 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
29 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
635 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
2154 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
1441 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
547 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
15 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