Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9296068 0.925 0.200 6 33020918 intergenic variant T/G snv 0.42 2
rs1058587 0.882 0.200 19 18388612 missense variant C/G;T snv 0.24; 9.1E-06 4
rs130067 0.851 0.200 6 31150734 missense variant T/G snv 0.23 0.21 4
rs2023305 0.851 0.280 6 167111410 intron variant C/T snv 0.38 4
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 5
rs13119723 0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs208294 0.790 0.320 12 121162450 missense variant T/A;C;G snv 0.51 9
rs2082940 0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv 10
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs4644 0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48