Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
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
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs333 0.667 0.520 3 46373453 frameshift variant GTCAGTATCAATTCTGGAAGAATTTCCAGACA/- delins 7.3E-02 23
rs1800630 0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs1800972 0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs1799946 0.732 0.360 8 6877909 5 prime UTR variant C/T snv 0.36 0.41 13
rs1333042 0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs1042229 0.790 0.280 19 51746419 missense variant A/C;G snv 0.32; 0.13 7
rs6596473 0.807 0.120 5 139374887 intron variant G/C;T snv 7
rs496892 0.827 0.160 9 22024352 intron variant C/T snv 0.40 6
rs3218977 0.807 0.240 2 102024739 3 prime UTR variant A/G snv 0.14 6
rs3811046 0.851 0.160 2 112913801 missense variant G/A;T snv 4.0E-06; 0.71 5
rs35068180 0.851 0.040 11 102845217 upstream gene variant A/-;AA delins 5