Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06 21
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs148704956 0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs16906252 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs2297518 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205