Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs41423247 0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22