rs75848804, 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.
Congenital hypofibrinogenemia
CUI: C2584774
Disease: Congenital hypofibrinogenemia
10 0.882 0.080 4 154604995 missense variant G/A;C;T snv 0.700 1.000 1 2015 2015
Fibrinogen Deficiency
CUI: C4316812
Disease: Fibrinogen Deficiency
4 0.882 0.080 4 154604995 missense variant G/A;C;T snv 0.010 1.000 1 2015 2015
Hypofibrinogenemia
CUI: C0553681
Disease: Hypofibrinogenemia
14 0.882 0.080 4 154604995 missense variant G/A;C;T snv 0.010 1.000 1 2015 2015
Storage disease
CUI: C0267971
Disease: Storage disease
1 0.882 0.080 4 154604995 missense variant G/A;C;T snv 0.010 1.000 1 2006 2006