Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9
rs2736108 0.807 0.160 5 1297373 upstream gene variant C/T snv 0.24 6
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 6
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs3132610 0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 6
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1682111 0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs3136820 0.776 0.200 14 20456995 missense variant T/A;C;G snv 8
rs3136817 0.732 0.280 14 20456275 intron variant T/C snv 0.23 12
rs3816358 0.827 0.120 11 13369925 intron variant C/A;T snv 5
rs3816360 0.807 0.120 11 13346203 intron variant T/C snv 0.58 6
rs200847762 0.790 0.160 6 32129371 missense variant G/A snv 2.7E-04 1.4E-05 7
rs10514231 0.807 0.160 5 82011593 intron variant C/T snv 0.56 6
rs1864182 0.827 0.120 5 82253421 missense variant C/A;G snv 0.59 0.47 6
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs624366
ATM
0.827 0.120 11 108283370 intron variant G/C snv 0.52 6