rs6050, FGA

N. diseases: 10
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.
Fibrinogen assay
CUI: C0337428
Disease: Fibrinogen assay
143 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.800 1.000 1 2011 2011
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.710 1.000 2 2006 2011
fibrinogen activity
CUI: C1325327
Disease: fibrinogen activity
63 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.700 1.000 1 2011 2011
Fibrinogen, CTCAE
CUI: C1561955
Disease: Fibrinogen, CTCAE
63 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.700 1.000 1 2011 2011
Venous Thrombosis
CUI: C0042487
Disease: Venous Thrombosis
218 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.700 1.000 1 2012 2012
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.030 0.667 3 2013 2016
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.020 1.000 2 2012 2016
Cardioembolism (high-risk/medium-risk)
4 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.010 1.000 1 2013 2013
Large-artery atherosclerosis (embolus/thrombosis)
35 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.010 1.000 1 2013 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.010 1.000 1 2009 2009