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
rs1862214 0.882 0.080 19 32544943 intergenic variant G/A;C snv 4
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 7
rs4769793 0.807 0.120 13 29985289 intergenic variant G/C snv 8
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
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
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
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs139293 0.882 0.080 22 39100331 missense variant G/A;T snv 2.3E-04; 0.27 4
rs533748068 0.851 0.080 1 155950962 missense variant C/A;T snv 4.3E-06 7.0E-06 5
rs1864182 0.827 0.120 5 82253421 missense variant C/A;G snv 0.59 0.47 6
rs1864183 0.742 0.240 5 82253397 missense variant C/T snv 0.52 0.40 12
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
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
rs767935771
AXL
0.827 0.080 19 41259690 missense variant T/C snv 1.6E-05 5.6E-05 6