Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs4464148 0.827 0.120 18 48932662 intron variant T/C snv 0.25 7
rs2270916 0.851 0.120 3 122282252 intron variant T/C snv 0.13 0.11 6
rs60745952 0.925 0.080 4 148827842 intron variant T/C snv 0.13 6
rs2736118 0.882 0.120 5 1260080 intron variant T/C snv 0.33 4
rs2737 0.851 0.080 17 47981705 missense variant T/C snv 0.25 0.19 4
rs2304204 0.882 0.160 19 49665763 5 prime UTR variant T/C snv 0.39 3
rs4147542 0.882 0.160 4 99347396 intron variant T/C snv 0.33 3
rs6474387 0.882 0.080 8 42328734 intron variant T/C snv 0.76 3
rs1450640054 0.925 0.080 7 45921122 missense variant T/C snv 1.0E-05 2
rs17109924 0.925 0.080 12 71584007 missense variant T/C snv 7.4E-02 8.6E-02 2
rs1724120 0.925 0.080 2 96143592 3 prime UTR variant T/C snv 0.53 2
rs2099902 0.925 0.080 10 52766089 3 prime UTR variant T/C snv 0.33 2
rs2470144 0.925 0.080 15 51329528 intron variant T/C snv 0.60 2
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 14
rs8905 0.925 0.080 17 68531661 3 prime UTR variant T/A;G snv 2
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs2228612 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 12
rs4939827 0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs4696480 0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs67376798 0.851 0.120 1 97082391 missense variant T/A snv 2.8E-03 3.3E-03 9
rs1057519822 0.925 0.080 15 66481818 missense variant T/A snv 3
rs4648110 0.925 0.080 4 102612664 intron variant T/A snv 0.22 3