Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs35761398 0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1419881 0.851 0.280 6 31162816 3 prime UTR variant G/A snv 0.50 4
rs3130542 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 8
rs2853953 1.000 0.080 6 31267728 downstream gene variant G/A snv 0.20 1
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs1800630 0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1800750
TNF
0.827 0.280 6 31575186 upstream gene variant G/A snv 1.6E-02 5
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 7
rs652888 0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10
rs12614 0.851 0.160 6 31946402 missense variant C/G;T snv 4.1E-06; 0.12 5
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs422951 0.807 0.280 6 32220606 missense variant T/C snv 0.40 0.40 8
rs9275319 0.807 0.200 6 32698518 intergenic variant A/G snv 0.15 6
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs9276370 0.882 0.200 6 32739518 upstream gene variant G/T snv 0.51 3
rs7756516 0.851 0.280 6 32756140 3 prime UTR variant C/T snv 0.49 4
rs7453920 0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs378352 0.925 0.200 6 33007157 synonymous variant G/A;C snv 0.20 2
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16