Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs61839660 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs3134792 0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 4
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs2295827 0.851 0.200 14 52708263 intron variant C/T snv 9.6E-02 9.1E-02 4
rs2647044 0.882 0.240 6 32700133 intergenic variant G/A snv 0.10 3
rs2295826 0.851 0.200 14 52708205 intron variant A/G snv 0.11 4
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs4613763 0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14 4
rs13222905 0.882 0.160 7 150566901 upstream gene variant G/A snv 0.15 3
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs6534349 0.925 0.160 4 122481040 intergenic variant A/G snv 0.17 2
rs6965571 0.882 0.160 7 150737384 5 prime UTR variant G/A snv 0.18 3
rs404860 0.925 0.160 6 32216568 non coding transcript exon variant T/C snv 0.21 2
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1131498 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs12150079 0.807 0.280 17 39869164 intron variant G/A snv 0.24 9