rs148685782, FGG

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.
Bleeding tendency
CUI: C1458140
Disease: Bleeding tendency
14 1.000 0.080 4 154611883 missense variant G/C snv 1.9E-03 2.2E-03 0.700 1.000 1 2019 2019
Fibrinogen assay
CUI: C0337428
Disease: Fibrinogen assay
143 1.000 0.080 4 154611883 missense variant G/C snv 1.9E-03 2.2E-03 0.700 1.000 1 2016 2016
Glycine measurement
CUI: C0523677
Disease: Glycine measurement
68 1.000 0.080 4 154611883 missense variant G/C snv 1.9E-03 2.2E-03 0.700 1.000 1 2019 2019
Congenital hypofibrinogenemia
CUI: C2584774
Disease: Congenital hypofibrinogenemia
10 1.000 0.080 4 154611883 missense variant G/C snv 1.9E-03 2.2E-03 0.700 0