Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs9271588 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 6
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs114050631 2 218156235 regulatory region variant C/T snv 6.9E-03 5
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs12542907 8 67900953 intergenic variant C/G snv 0.29 5
rs12600856 17 40007042 intergenic variant T/C;G snv 5
rs200638392 6 87128241 intergenic variant GAT/-;GATGAT delins 0.47 5
rs201950044 1 161639782 intergenic variant G/T snv 5
rs2082382 5 148820990 upstream gene variant G/A snv 0.72 5
rs2338224 5 72432861 intergenic variant A/G snv 0.85 5
rs34762051 17 40007650 downstream gene variant AA/-;A;AAA delins 0.31 5
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5