Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs121909607
FGA
0.882 0.160 4 154589513 missense variant C/T snv 1.2E-05 1.4E-05 4
rs121909606
FGA
0.925 0.080 4 154589514 missense variant G/A snv 4.0E-06 7.0E-06 2
rs1276352833
FGA
0.925 0.080 4 154586057 missense variant G/A;T snv 4.0E-06; 4.0E-06 2
rs121913087
FGG
0.925 0.080 4 154606933 missense variant G/A snv 2
rs778686781
PLG
1.000 0.080 6 160718329 missense variant T/C snv 4.0E-06 1