Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36