Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121909607
rs121909607
FGA
4 0.882 0.160 4 154589513 missense variant C/T snv 1.2E-05 1.4E-05 0.710 1.000 1 2013 2013
dbSNP: rs121909606
rs121909606
FGA
2 0.925 0.080 4 154589514 missense variant G/A snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs121913087
rs121913087
FGG
2 0.925 0.080 4 154606933 missense variant G/A snv 0.010 1.000 1 2015 2015
dbSNP: rs1276352833
rs1276352833
FGA
2 0.925 0.080 4 154586057 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs6025
rs6025
F5
43 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2000 2000
dbSNP: rs778686781
rs778686781
PLG
1 1.000 0.080 6 160718329 missense variant T/C snv 4.0E-06 0.010 1.000 1 2000 2000