Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs852426 0.882 0.240 7 5526722 downstream gene variant C/T snv 0.39 5
rs16835198 0.882 0.200 1 32861080 downstream gene variant G/T snv 0.29 3
rs1942872 0.925 0.160 18 60201132 downstream gene variant C/T snv 0.21 2
rs499765 0.925 0.160 19 48763133 downstream gene variant C/G snv 0.45 2
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1800630 0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs11771443 0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 8
rs4783961 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 7
rs34713741 0.882 0.280 15 101277671 upstream gene variant C/A;T snv 0.24 3
rs7222331 0.925 0.120 17 40995605 upstream gene variant C/T snv 0.24 3
rs1888747 1.000 0.120 9 83540636 upstream gene variant C/G snv 0.78 2
rs11886047 1.000 0.120 2 43623451 upstream gene variant T/A;C snv 0.20 1
rs2346061 1.000 0.120 18 74533297 upstream gene variant C/A snv 0.71 1
rs3752462 0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 7
rs765798193 0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs1275805226
AGT
0.776 0.240 1 230706148 frameshift variant G/- del 7.0E-06 12