Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140693 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 10
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs3219175 0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02 10
rs7775397 0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 7
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs389884 0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 10
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs1270942 0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs558702 0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs3115672 0.851 0.200 6 31760120 synonymous variant C/T snv 6.4E-02 7.9E-02 4
rs3131379 0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 10
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs3134942 0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11 7
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs2257914 0.925 0.200 6 30152786 3 prime UTR variant C/A snv 0.17 2
rs2281089 0.851 0.200 22 37136132 intron variant A/G snv 0.17 4
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135