Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9904341 0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs9350 0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs914956206 0.882 0.080 6 43770762 missense variant G/A;T snv 4
rs909797662 0.790 0.120 7 55191837 missense variant G/A snv 8
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs781172058 0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06 21
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs773919809 0.763 0.200 10 129766957 missense variant C/T snv 2.0E-05 13
rs770327175 0.851 0.120 2 136115878 missense variant C/A;T snv 8.0E-06 5
rs767741751 0.851 0.120 8 6562846 missense variant C/A snv 4.0E-06 5
rs766914563 0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs756045117 0.925 0.080 3 37012090 missense variant C/G;T snv 1.6E-05 3
rs755100942 0.724 0.320 13 49630894 stop gained G/A snv 4.2E-06 17