Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799810 1.000 0.040 2 127418464 5 prime UTR variant A/T snv 0.38 0.44 5
rs10485505 1.000 0.080 20 34437762 intron variant C/G;T snv 3
rs1158867 1.000 0.080 2 127419801 splice region variant C/T snv 0.51 3
rs1799808 1.000 0.040 2 127418286 upstream gene variant C/T snv 0.33 3
rs1885119 1.000 0.080 20 35057846 intron variant T/C snv 0.58 3
rs2065108 1.000 0.080 20 35119019 intron variant C/T snv 0.61 3
rs3736802 1.000 0.080 20 35016239 intron variant T/C snv 0.53 3
rs3818253 1.000 0.040 20 35009073 intron variant G/A snv 0.19 3
rs4150407 1.000 0.120 2 127292055 3 prime UTR variant T/C snv 0.47 3
rs6060038 1.000 0.080 20 34769912 intron variant G/A snv 0.45 3
rs6087664 1.000 0.080 20 35038413 intron variant C/A;G;T snv 3
rs6088343 1.000 0.040 20 33908259 downstream gene variant C/T snv 0.46 3
rs6088590 1.000 0.040 20 34725762 intron variant T/C snv 0.36 3
rs6088662 1.000 0.040 20 34959830 intron variant T/G snv 0.20 3
rs6088692 1.000 0.080 20 35050785 intron variant A/G snv 0.58 3
rs6088727 1.000 0.080 20 35125836 intron variant G/A snv 0.51 3
rs6120816 1.000 0.080 20 35056555 intron variant G/A;C snv 3
rs6141509 1.000 0.080 20 34731584 intron variant G/A snv 0.45 3
rs6142044 1.000 0.040 20 33918789 intergenic variant A/T snv 0.47 3
rs2068834 0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs1178977 0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21 7
rs7811265 0.925 0.120 7 73520180 intron variant A/G snv 0.23 7
rs1178979 0.925 0.120 7 73442100 3 prime UTR variant T/C snv 0.21 6
rs17145713 0.925 0.120 7 73490480 intron variant C/T snv 0.21 6
rs1919127 0.925 0.120 2 27578626 missense variant T/C snv 0.31 0.27 6