Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs7096206 0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs2606345 0.732 0.360 15 74724835 intron variant C/A snv 0.46 16
rs1800972 0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs11362 0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs1799946 0.732 0.360 8 6877909 5 prime UTR variant C/T snv 0.36 0.41 13
rs61330082 0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs149989682 0.790 0.240 16 2317763 missense variant T/A;C snv 2.3E-03 10
rs315952 0.763 0.400 2 113132727 missense variant T/A;C snv 4.0E-06; 0.31 10
rs1130866 0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 9
rs1805018 0.827 0.200 6 46711566 missense variant A/G snv 6.8E-02 0.10 6
rs1965708 0.851 0.200 10 79557289 missense variant G/T snv 0.22 0.25 6
rs533117495 0.827 0.200 7 87595783 missense variant C/T snv 8.0E-06 5
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5