Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 117
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 60
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 27
rs1801198 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs1800975
XPA
0.701 0.360 9 97697296 5 prime UTR variant T/C;G snv 0.63; 4.5E-06; 4.5E-06 19
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 17
rs770460061 0.742 0.240 11 67585239 missense variant T/C;G snv 4.0E-06; 1.2E-05 14
rs7775 0.732 0.240 2 182834857 missense variant G/A;C;T snv 8.0E-05; 8.0E-02; 5.6E-05 13
rs1057910 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 12
rs927650 0.763 0.240 20 54156202 intron variant T/A;C snv 9
rs1245554802 0.851 0.120 3 9765892 splice acceptor variant T/C snv 4.0E-06 5
rs771306418 0.851 0.120 3 9765885 splice acceptor variant -/C delins 5
rs2287939 0.851 0.160 5 33998778 missense variant A/C;G snv 1.6E-05; 0.70 4
rs8044769
FTO
0.851 0.200 16 53805223 intron variant T/A;C;G snv 4