Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs2395029 0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12
rs10484554 0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs241447 0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 11
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 10
rs3130380 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs9261290 0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 9
rs12198173 0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs2894207 0.882 0.160 6 31295974 intron variant T/C snv 0.20 8
rs3815087 0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 8
rs3823418 0.925 0.120 6 31133165 intron variant G/A snv 0.23 8
rs9368699 0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 8
rs2516509 0.882 0.160 6 31482217 intron variant T/C snv 0.19 7