Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs12778366
SIRT1
0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs11886868
BCL11A
0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 12
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 11
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 9
rs17045754
LOC105374610 ; ACYP2
0.790 0.280 2 54269620 intron variant G/A;C snv 7
rs770140945
CYP1A1
0.882 0.200 15 74720665 missense variant G/A snv 4.0E-06 7.0E-06 4