Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1482856709 0.925 0.080 3 93900887 missense variant G/A snv 3
rs1431515214
APC
0.925 0.080 5 112839790 missense variant G/A snv 4.0E-06 2
rs780225764
F2
1.000 0.080 11 46726797 missense variant A/G snv 4.0E-06 2
rs911028477 1.000 0.080 16 27362773 missense variant G/A snv 2
rs370975770 1.000 0.080 22 38115666 missense variant C/T snv 8.9E-06 2.8E-05 1
rs751437628 1.000 0.080 20 23048698 synonymous variant G/A;C snv 9.9E-06; 9.9E-06 1
rs766760828 1.000 0.080 22 38140060 missense variant A/G snv 4.0E-06 1
rs780767010 1.000 0.080 1 11796282 missense variant G/A snv 8.0E-06 1
rs866316103
PC
1.000 0.080 11 66872069 missense variant G/A snv 7.0E-06 1
rs121908686 0.882 0.120 22 38112558 missense variant C/T snv 9.0E-05 6
rs1371086615
APC
0.851 0.120 5 112828890 missense variant G/A snv 4.0E-06 7.0E-06 4
rs765557332
APC
0.851 0.120 5 112835075 missense variant G/A snv 7.0E-06 4
rs878853423
APC
0.851 0.120 5 112837663 missense variant G/A snv 4
rs1255283120 0.807 0.160 1 11792345 missense variant G/A snv 4.0E-06 7.0E-06 7
rs1312546120
F5
0.807 0.160 1 169541191 missense variant T/C snv 4.0E-06 7
rs144246695 0.851 0.160 4 83310887 missense variant G/A snv 8.0E-06 4
rs575231506 0.925 0.160 4 2894667 missense variant C/A;T snv 4.1E-06; 4.1E-06 2
rs749785846
FGB
0.925 0.160 4 154568469 synonymous variant C/T snv 4.0E-06 2
rs552953108
F2
0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 16
rs747418061
APC
0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 10
rs777692567 0.827 0.200 8 42182845 missense variant G/A snv 4.0E-05 1.4E-05 5
rs1369837875 0.882 0.200 22 38128276 synonymous variant G/A snv 4
rs3789683
F3
0.925 0.200 1 94530506 missense variant C/T snv 6.5E-03 1.0E-02 3
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs368927897 0.790 0.240 9 5072541 missense variant G/A;T snv 2.8E-05; 6.4E-05 9