Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 17
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17878467 0.925 0.080 17 78214076 upstream gene variant C/G;T snv 6
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 117
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 35
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 47
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 15
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 24
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 114
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 221
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06 21
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134