Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs3130542 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 8
rs2853953 1.000 0.080 6 31267728 downstream gene variant G/A snv 0.20 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs1800630 0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs61330082 0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs510432 0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs1800750
TNF
0.827 0.280 6 31575186 upstream gene variant G/A snv 1.6E-02 5
rs705382 0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53 5
rs7095891 0.882 0.120 10 52771701 upstream gene variant G/A snv 0.30 3
rs9276370 0.882 0.200 6 32739518 upstream gene variant G/T snv 0.51 3
rs3806798 0.925 0.080 4 141636126 upstream gene variant T/A snv 8.7E-02 2
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1054690270 0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs9277535 0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs1053004 0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11