rs6054, FGB

N. diseases: 6
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 1.000 0.080 4 154568456 missense variant C/T snv 2.4E-03 2.7E-03 0.800 1.000 2 2011 2016
Bleeding tendency
CUI: C1458140
Disease: Bleeding tendency
14 1.000 0.080 4 154568456 missense variant C/T snv 2.4E-03 2.7E-03 0.700 1.000 1 2019 2019
fibrinogen activity
CUI: C1325327
Disease: fibrinogen activity
63 1.000 0.080 4 154568456 missense variant C/T snv 2.4E-03 2.7E-03 0.700 1.000 1 2011 2011
Fibrinogen, CTCAE
CUI: C1561955
Disease: Fibrinogen, CTCAE
63 1.000 0.080 4 154568456 missense variant C/T snv 2.4E-03 2.7E-03 0.700 1.000 1 2011 2011
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 1.000 0.080 4 154568456 missense variant C/T snv 2.4E-03 2.7E-03 0.700 1.000 1 2017 2017
Congenital hypofibrinogenemia
CUI: C2584774
Disease: Congenital hypofibrinogenemia
10 1.000 0.080 4 154568456 missense variant C/T snv 2.4E-03 2.7E-03 0.700 0