rs5985, F13A1

N. diseases: 20
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.
Coagulation factor measurement
CUI: C1167912
Disease: Coagulation factor measurement
26 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.700 1.000 1 2013 2013
von Willebrand's factor (lab test)
CUI: C2239219
Disease: von Willebrand's factor (lab test)
427 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.700 1.000 1 2013 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.040 1.000 4 2002 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.030 0.667 3 2002 2009
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.030 0.667 3 2002 2009
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.030 0.667 3 2002 2009
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.030 1.000 3 2002 2016
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.020 1.000 2 2006 2014
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.010 1.000 1 2018 2018
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.010 1.000 1 2011 2011
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.010 1 2002 2002
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.010 1 2002 2002
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.010 1.000 1 2016 2016
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.010 1.000 1 2002 2002
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.010 1.000 1 2011 2011
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.010 1.000 1 2002 2002
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.010 1.000 1 2011 2011
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.010 1 2002 2002
Peripheral Vascular Diseases
CUI: C0085096
Disease: Peripheral Vascular Diseases
18 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.010 1.000 1 2002 2002
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 0.010 1.000 1 2019 2019