Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs13119723 0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs130067 0.851 0.200 6 31150734 missense variant T/G snv 0.23 0.21 4
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63