rs899127658, F2

N. diseases: 82
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.
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.547 0.720 11 46739084 missense variant G/A;C snv 0.100 0.970 33 1999 2019
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.547 0.720 11 46739084 missense variant G/A;C snv 0.100 1.000 15 1999 2019
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.547 0.720 11 46739084 missense variant G/A;C snv 0.100 1.000 12 1999 2010
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.547 0.720 11 46739084 missense variant G/A;C snv 0.090 1.000 9 1999 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.547 0.720 11 46739084 missense variant G/A;C snv 0.040 1.000 4 2002 2009
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.547 0.720 11 46739084 missense variant G/A;C snv 0.040 0.750 4 2002 2010
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.547 0.720 11 46739084 missense variant G/A;C snv 0.040 1.000 4 1999 2013
Miscarriage
CUI: C4552766
Disease: Miscarriage
56 0.547 0.720 11 46739084 missense variant G/A;C snv 0.040 1.000 4 2002 2016
Portal Vein Thrombosis
CUI: C0155773
Disease: Portal Vein Thrombosis
8 0.547 0.720 11 46739084 missense variant G/A;C snv 0.040 1.000 4 1999 2015
Protein C Deficiency
CUI: C0398625
Disease: Protein C Deficiency
14 0.547 0.720 11 46739084 missense variant G/A;C snv 0.040 1.000 4 1999 2017
Prothrombin G20210A mutation
CUI: C2584409
Disease: Prothrombin G20210A mutation
9 0.547 0.720 11 46739084 missense variant G/A;C snv 0.040 0.750 4 1999 2018
prothrombin gene mutation
CUI: C1260403
Disease: prothrombin gene mutation
5 0.547 0.720 11 46739084 missense variant G/A;C snv 0.040 1.000 4 1998 2012
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.547 0.720 11 46739084 missense variant G/A;C snv 0.030 1.000 3 2000 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.547 0.720 11 46739084 missense variant G/A;C snv 0.030 1.000 3 1999 2016
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.547 0.720 11 46739084 missense variant G/A;C snv 0.030 0.667 3 1999 2005
Protein S Deficiency
CUI: C0242666
Disease: Protein S Deficiency
14 0.547 0.720 11 46739084 missense variant G/A;C snv 0.030 1.000 3 2003 2017
Activated Protein C Resistance
CUI: C0600433
Disease: Activated Protein C Resistance
30 0.547 0.720 11 46739084 missense variant G/A;C snv 0.020 1.000 2 1996 2018
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.547 0.720 11 46739084 missense variant G/A;C snv 0.020 1.000 2 1999 2018
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.547 0.720 11 46739084 missense variant G/A;C snv 0.020 1.000 2 2010 2011
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.547 0.720 11 46739084 missense variant G/A;C snv 0.020 1.000 2 1999 2018
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.547 0.720 11 46739084 missense variant G/A;C snv 0.020 1.000 2 2006 2013
Antithrombin III Deficiency
CUI: C0272375
Disease: Antithrombin III Deficiency
52 0.547 0.720 11 46739084 missense variant G/A;C snv 0.020 1.000 2 2000 2017
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.547 0.720 11 46739084 missense variant G/A;C snv 0.020 1.000 2 2003 2009
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.547 0.720 11 46739084 missense variant G/A;C snv 0.020 1.000 2 1999 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.547 0.720 11 46739084 missense variant G/A;C snv 0.020 0.500 2 2004 2009