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
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs3842 0.882 0.080 7 87504050 3 prime UTR variant T/C snv 0.16 5
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
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
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
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs664677
ATM
0.807 0.160 11 108272455 intron variant C/A;T snv 0.65 8
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
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
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25