Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs2890565 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 15
rs121908212 0.732 0.160 19 13303877 missense variant G/A snv 14
rs228648 0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs10994336 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs12273363 0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs1950902 0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs11172113 0.882 0.080 12 57133500 intron variant T/C snv 0.42 10
rs2271933 0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50 9
rs344781 0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 7
rs2049046 0.827 0.200 11 27702228 intron variant T/A snv 0.48 6
rs1835740 0.882 0.040 8 97154685 intergenic variant T/C snv 0.75 5
rs28933696 0.882 0.160 19 15192134 missense variant G/A snv 5
rs2651899 0.882 0.040 1 3167148 intron variant T/A;C snv 5
rs1800750
TNF
0.827 0.280 6 31575186 upstream gene variant G/A snv 1.6E-02 5