Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs780225764
F2
1.000 0.080 11 46726797 missense variant A/G snv 4.0E-06 2
rs766760828 1.000 0.080 22 38140060 missense variant A/G snv 4.0E-06 1
rs141012637 0.851 0.320 18 63901881 stop gained C/A;T snv 7.0E-05 4
rs575231506 0.925 0.160 4 2894667 missense variant C/A;T snv 4.1E-06; 4.1E-06 2
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs121908686 0.882 0.120 22 38112558 missense variant C/T snv 9.0E-05 6
rs3789683
F3
0.925 0.200 1 94530506 missense variant C/T snv 6.5E-03 1.0E-02 3
rs749785846
FGB
0.925 0.160 4 154568469 synonymous variant C/T snv 4.0E-06 2
rs370975770 1.000 0.080 22 38115666 missense variant C/T snv 8.9E-06 2.8E-05 1
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 25
rs552953108
F2
0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 16
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs747418061
APC
0.807 0.200 5 112828920 missense variant G/A snv 3.2E-05 7.0E-06 10
rs1255283120 0.807 0.160 1 11792345 missense variant G/A snv 4.0E-06 7.0E-06 7
rs777692567 0.827 0.200 8 42182845 missense variant G/A snv 4.0E-05 1.4E-05 5
rs779829591
F3
0.827 0.320 1 94532395 missense variant G/A snv 4.0E-06 5
rs1369837875 0.882 0.200 22 38128276 synonymous variant G/A snv 4
rs1371086615
APC
0.851 0.120 5 112828890 missense variant G/A snv 4.0E-06 7.0E-06 4