Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057519853 0.851 0.080 9 77794572 missense variant TG/AA mnv 6
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 47
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs2015 0.925 0.120 19 38878729 3 prime UTR variant T/G snv 0.47 3
rs72478580 1.000 5 35072610 missense variant T/G snv 1.9E-02 1.9E-02 1
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 60
rs3803185 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19
rs1202989817 0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs2229992
APC
0.827 0.200 5 112827157 stop gained T/C;G snv 0.58 0.47 5
rs112295309 1.000 0.080 8 143813896 missense variant T/C;G snv 6.1E-04 3
rs121912518 0.882 0.160 2 48688064 missense variant T/C;G snv 3
rs169724
SYK
9 90828217 intron variant T/C;G snv 1
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 153
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29