Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs406193 0.882 0.120 20 32811837 downstream gene variant T/C snv 0.91 5
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 9
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs822395 0.776 0.240 3 186849018 intron variant C/A;G snv 10
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs117251022 0.827 0.120 13 49630641 missense variant G/A;C;T snv 8.8E-05; 1.9E-03 5
rs34301344 0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs3803185 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19
rs755100942 0.724 0.320 13 49630894 stop gained G/A snv 4.2E-06 17
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 11
rs758081262
ATM
0.851 0.360 11 108267258 stop gained C/T snv 1.2E-05 4
rs768362387
ATM
0.851 0.360 11 108253846 stop gained C/A snv 5
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs2240308 0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18