Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1950902 0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs1046428 0.776 0.200 14 77327940 missense variant T/A;C snv 4.0E-06; 0.81 8
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 14
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2227564 0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
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
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs351771
APC
0.882 0.120 5 112828864 synonymous variant G/A snv 0.65 0.59 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2180314 0.776 0.200 6 52752933 missense variant C/G snv 0.60 0.52 8
rs6166 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 17
rs732774 0.827 0.320 13 51949672 missense variant C/T snv 0.57 0.56 5
rs2424913 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs6165 0.724 0.160 2 48963902 missense variant C/G;T snv 4.0E-06; 0.55 14
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2228611 0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs2363956 0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 8
rs2240308 0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1057941 0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs1801243 0.851 0.200 13 51974004 missense variant A/C;T snv 0.44; 2.0E-05 4
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72