rs552953108, F2

N. diseases: 16
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 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.100 1.000 12 1998 2019
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.060 1.000 6 1999 2019
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.020 1.000 2 1996 1999
Activated Protein C Resistance
CUI: C0600433
Disease: Activated Protein C Resistance
30 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 1996 1996
Cooley's anemia
CUI: C0002875
Disease: Cooley's anemia
19 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 2002 2002
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 1998 1998
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 1999 1999
Isolated thrombocytopenia
CUI: C4511035
Disease: Isolated thrombocytopenia
9 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 2003 2003
Limb ischemia
CUI: C2945695
Disease: Limb ischemia
3 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 2009 2009
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 2010 2010
Nephrotic Syndrome
CUI: C0027726
Disease: Nephrotic Syndrome
45 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 1998 1998
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 2009 2009
Protein S Deficiency
CUI: C0242666
Disease: Protein S Deficiency
14 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 1996 1996
Retinal Vein Occlusion
CUI: C0035328
Disease: Retinal Vein Occlusion
15 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 2002 2002
Sinus Thrombosis, Intracranial
CUI: C0037198
Disease: Sinus Thrombosis, Intracranial
5 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 1998 1998
Thromboangiitis Obliterans
CUI: C0040021
Disease: Thromboangiitis Obliterans
16 0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 0.010 1.000 1 2000 2000