Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs16917496 0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs3923087 0.827 0.160 17 65553143 intron variant T/C snv 0.58 5
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs7958904 0.724 0.200 12 53963768 non coding transcript exon variant C/A;G snv 15
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
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 25
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33