rs121918027, PLG

N. diseases: 7
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.
Plasminogen Deficiency, Type I
CUI: C1968804
Disease: Plasminogen Deficiency, Type I
13 0.827 0.320 6 160738593 missense variant G/A snv 1.4E-03 3.5E-04 0.750 1.000 13 1982 2017
Antiphospholipid Syndrome
CUI: C0085278
Disease: Antiphospholipid Syndrome
17 0.827 0.320 6 160738593 missense variant G/A snv 1.4E-03 3.5E-04 0.010 1.000 1 2002 2002
Atypical Hemolytic Uremic Syndrome
CUI: C2931788
Disease: Atypical Hemolytic Uremic Syndrome
42 0.827 0.320 6 160738593 missense variant G/A snv 1.4E-03 3.5E-04 0.010 1.000 1 2016 2016
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.827 0.320 6 160738593 missense variant G/A snv 1.4E-03 3.5E-04 0.010 1.000 1 2003 2003
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.827 0.320 6 160738593 missense variant G/A snv 1.4E-03 3.5E-04 0.010 1.000 1 2013 2013
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.827 0.320 6 160738593 missense variant G/A snv 1.4E-03 3.5E-04 0.010 1.000 1 1997 1997
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.827 0.320 6 160738593 missense variant G/A snv 1.4E-03 3.5E-04 0.010 1.000 1 2017 2017