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
rs4646903 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 4
rs3931020 0.882 0.040 1 74769633 downstream gene variant T/C snv 0.71 4
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
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs1799998 0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs2227631 0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13