Disease: Hypofibrinogenemia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs75848804
FGG
0.882 0.080 4 154604995 missense variant G/A;C;T snv 4
rs1317589749
FGB
0.925 0.080 4 154570471 missense variant T/A snv 4.0E-06 2
rs772014512
FGB
0.925 0.080 4 154567772 missense variant C/T snv 4.8E-05 1.4E-05 2
rs894077860
FGB
0.925 0.080 4 154569660 stop gained C/T snv 2