rs761740955, FGB

N. diseases: 5
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.
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.827 0.200 4 154566637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2017 2017
Cardioembolic stroke
CUI: C1531624
Disease: Cardioembolic stroke
28 0.827 0.200 4 154566637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2017 2017
Cat eye syndrome
CUI: C0265493
Disease: Cat eye syndrome
6 0.827 0.200 4 154566637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2017 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.827 0.200 4 154566637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2009 2009
Prothrombin G20210A mutation
CUI: C2584409
Disease: Prothrombin G20210A mutation
9 0.827 0.200 4 154566637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2004 2004