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
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
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
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs11137037 0.851 0.200 8 6538661 intron variant A/C snv 0.40 4
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs2929970 0.827 0.200 8 133228894 3 prime UTR variant G/A snv 0.52 5
rs2929973 0.851 0.200 8 133230265 3 prime UTR variant G/T snv 0.85 5
rs62514004 0.790 0.240 8 133190246 upstream gene variant A/G snv 0.28 8
rs1535045 0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs11543848 0.790 0.240 7 55161562 missense variant G/A;C;T snv 7
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs1360485 0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108