Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs371057322 0.925 0.040 2 8793960 missense variant T/C snv 1.4E-05 2
rs6141 0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 4
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs750898115 0.882 0.080 4 75787191 missense variant A/G snv 1.0E-05 3.5E-05 4
rs4859584 1.000 0.040 4 76021984 intron variant G/C snv 0.61 0.61 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs3132468 0.827 0.240 6 31507709 intron variant C/T snv 0.77 5
rs5745568 0.882 0.080 6 33580617 intron variant G/T snv 0.19 4
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1285933 0.925 0.040 7 141927349 intron variant G/A snv 0.54 2
rs3739319 0.925 0.040 8 39927802 intron variant G/A snv 0.40 0.37 2
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9
rs669260 0.851 0.080 9 32503442 intron variant T/A;C snv 4
rs3205166 0.925 0.040 9 32459452 synonymous variant T/A;G snv 0.35 2
rs3765524 0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs3740360 0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 7
rs1447043692 0.925 0.040 10 98641918 missense variant C/T snv 2
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22