Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs2665390 0.776 0.160 3 156679960 intron variant C/T snv 0.92 8
rs1950902 0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 10
rs2227564 0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 12
rs2191249 0.882 0.120 17 61758503 intron variant T/G snv 0.79 3
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 8
rs851797 0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs238406 0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 24
rs495139 0.882 0.120 18 676008 intron variant G/C snv 0.63 4
rs1467465 0.827 0.160 1 27884892 non coding transcript exon variant A/G snv 0.61 7
rs351771
APC
0.882 0.120 5 112828864 synonymous variant G/A snv 0.65 0.59 3
rs230521 0.851 0.160 4 102542171 intron variant C/G snv 0.59 4
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 20
rs3923087 0.827 0.160 17 65553143 intron variant T/C snv 0.58 5
rs1836724 0.807 0.240 2 211380227 3 prime UTR variant G/A snv 0.57 6
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1256031 0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 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
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs9375701 0.827 0.160 6 130062912 intron variant C/T snv 0.53 6
rs2424913 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18