Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 7
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 5
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 4
rs121913105 0.653 0.600 4 1806163 missense variant A/C;T snv 4
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 4
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 4
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 4
rs61753793 0.851 0.120 2 47799002 missense variant T/C snv 3.6E-05 5.6E-05 3
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs63750664 0.882 0.200 2 47783292 missense variant C/A;T snv 4.1E-06; 9.4E-05 3
rs2020912 0.807 0.480 2 47800616 missense variant T/C;G snv 5.1E-03 3
rs121913272 0.752 0.400 3 179210192 missense variant T/C;G snv 3
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs4148323 0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 3
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs397514606 0.763 0.320 1 243695714 missense variant C/T snv 2
rs1400295986
APC
0.925 0.080 5 112838233 missense variant T/C snv 2
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 2
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 2
rs267608140 0.925 0.160 2 47806838 missense variant T/A;C snv 2
rs3211299 0.882 0.200 2 47791097 missense variant G/T snv 9.4E-04 1.5E-03 2
rs63749973 0.925 0.160 2 47799679 stop gained G/A;T snv 2.4E-04 2.8E-05 2
rs63750389 0.925 0.160 2 47800532 missense variant A/G snv 8.0E-06 2