Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs147377392 0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs747418061
APC
0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 10
rs1926447 0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 10
rs1131012 0.763 0.280 17 64350416 missense variant T/C snv 0.38 10
rs121918474 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 10
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 9
rs12953 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs2000813 0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 8
rs13306190 0.807 0.320 2 21032408 missense variant G/A;C;T snv 1.7E-04; 8.0E-06 7
rs1255283120 0.807 0.160 1 11792345 missense variant G/A snv 4.0E-06 7.0E-06 7
rs121918027
PLG
0.827 0.320 6 160738593 missense variant G/A snv 1.4E-03 3.5E-04 7
rs200960801 0.827 0.200 6 151944488 missense variant A/G snv 4.0E-06 6
rs6050
FGA
0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 6
rs1613662 0.851 0.120 19 55025227 missense variant G/A snv 0.85 0.83 6
rs9797861 0.790 0.200 19 10632450 intron variant C/A;G;T snv 6
rs2036914
F11
0.882 0.160 4 186271327 intron variant T/C snv 0.57 4
rs121909613
FGA
0.882 0.160 4 154585712 splice acceptor variant G/A;C;T snv 4.8E-05; 4.0E-06 4
rs4987262 0.882 0.040 19 46623592 missense variant G/A;C snv 7.1E-03 4
rs1800386
VWF
0.851 0.120 12 6018667 missense variant T/C snv 2.7E-03 2.3E-03 4
rs747301897 1.000 0.040 19 45363999 synonymous variant G/A snv 7.1E-06 3
rs6507931 0.882 0.080 18 49586638 intron variant C/T snv 0.52 3
rs5940 0.882 0.080 2 187466977 missense variant C/T snv 1.3E-02 1.4E-02 3
rs764948729
PLG
0.925 0.080 6 160731092 missense variant A/C snv 4.0E-06 3
rs121918146 0.827 0.200 2 127428485 missense variant G/A snv 1.2E-05 2.1E-05 3