Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 1
rs1566734 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 1
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 1
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 10
rs121913502 0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 6
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs121913331
APC
0.851 0.120 5 112838934 stop gained C/A;T snv 8.0E-06 5
rs759610249 0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 12
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 5
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 14
rs772110575 0.807 0.160 3 179198938 missense variant G/A;T snv 4.0E-06 6
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 19
rs747241612 0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs747342068 0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17