Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs67397200 0.827 0.160 19 17290595 upstream gene variant C/G snv 0.27 5
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs387906659 0.742 0.280 19 40257052 stop gained C/A;T snv 14
rs397514606 0.763 0.320 1 243695714 missense variant C/T snv 14
rs2363956 0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 8
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
rs34301344 0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
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
rs2240308 0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs8170 0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 13
rs28997576 0.776 0.160 2 214752454 missense variant C/G;T snv 1.5E-02 11
rs200389141
BLM
0.776 0.320 15 90761015 stop gained C/A;T snv 4.1E-06; 1.4E-04 1.7E-04 11
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1799950 0.752 0.240 17 43094464 missense variant T/C snv 4.7E-02 4.6E-02 13
rs1800709 0.851 0.160 17 43093010 missense variant G/A snv 1.7E-03 1.4E-03 6
rs1800751 0.851 0.160 17 43047676 missense variant G/A;C snv 4.0E-06 5
rs190900046 0.827 0.160 17 43104197 synonymous variant A/C snv 8.0E-06 4.2E-05 5
rs273900729 0.925 0.160 17 43082529 missense variant A/G snv 2