rs121909607, FGA

N. diseases: 4
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.
Dysfibrinogenemia
CUI: C1260903
Disease: Dysfibrinogenemia
6 0.882 0.160 4 154589513 missense variant C/T snv 1.2E-05 1.4E-05 0.710 1.000 1 2013 2013
Bleeding tendency
CUI: C1458140
Disease: Bleeding tendency
14 0.882 0.160 4 154589513 missense variant C/T snv 1.2E-05 1.4E-05 0.700 1.000 1 2019 2019
Hypofibrinogenemia
CUI: C0553681
Disease: Hypofibrinogenemia
14 0.882 0.160 4 154589513 missense variant C/T snv 1.2E-05 1.4E-05 0.700 1.000 1 2019 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.882 0.160 4 154589513 missense variant C/T snv 1.2E-05 1.4E-05 0.010 1.000 1 2019 2019