Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs132793 0.851 0.160 22 41667677 downstream gene variant A/C;G;T snv 7
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs765189442 0.925 0.080 2 168995422 missense variant T/C snv 8.1E-06 4
rs17822931 0.827 0.080 16 48224287 missense variant C/G;T snv 4.0E-06; 0.22 0.13 7
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
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
rs2229992
APC
0.827 0.200 5 112827157 stop gained T/C;G snv 0.58 0.47 6
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
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
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs13010627 0.807 0.280 2 201209375 missense variant G/A snv 4.2E-02 4.3E-02 10
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42