rs751377893, F5

N. diseases: 65
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 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.100 0.966 29 1996 2019
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.100 1.000 13 1995 2019
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.100 1.000 10 1999 2019
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.070 1.000 7 2000 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.040 1.000 4 1995 2018
prothrombin gene mutation
CUI: C1260403
Disease: prothrombin gene mutation
5 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.040 1.000 4 2005 2012
Activated Protein C Resistance
CUI: C0600433
Disease: Activated Protein C Resistance
30 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.030 1.000 3 1995 2018
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.030 1.000 3 1996 2013
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.030 0.667 3 1995 2009
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.030 0.667 3 1995 2009
Miscarriage
CUI: C4552766
Disease: Miscarriage
56 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.030 1.000 3 2005 2016
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.020 1.000 2 2010 2016
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.020 1.000 2 2006 2013
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.020 1.000 2 2006 2013
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.020 1.000 2 2002 2002
Portal Vein Thrombosis
CUI: C0155773
Disease: Portal Vein Thrombosis
8 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.020 1.000 2 2005 2015
Protein S Deficiency
CUI: C0242666
Disease: Protein S Deficiency
14 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.020 1.000 2 2006 2017
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.020 0.500 2 2006 2011
Vertical Talus
CUI: C0240912
Disease: Vertical Talus
20 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.020 1.000 2 2011 2012
5,10-Methylenetetrahydrofolate reductase deficiency
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
6 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.010 1.000 1 2008 2008
Amaurosis Fugax
CUI: C0149793
Disease: Amaurosis Fugax
2 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.010 1.000 1 2009 2009
Antithrombin III Deficiency
CUI: C0272375
Disease: Antithrombin III Deficiency
52 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.010 1.000 1 2017 2017
Arterial Occlusive Diseases
CUI: C0003838
Disease: Arterial Occlusive Diseases
4 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.010 1.000 1 1999 1999
beta Thalassemia
CUI: C0005283
Disease: beta Thalassemia
103 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.010 1.000 1 2008 2008
Beta thalassemia intermedia
CUI: C0472767
Disease: Beta thalassemia intermedia
12 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.010 1.000 1 2008 2008