Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 6
rs2856997 0.882 0.200 6 32813999 non coding transcript exon variant C/A snv 0.45 6
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs3115663 0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 6
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs3130618 0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs3131296 0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs3131379 0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 6
rs3132580 0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 6
rs3134942 0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11 6
rs558702 0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs652888 0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 6
rs660895 0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 6
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs6906662 0.882 0.200 6 32298729 intron variant G/A snv 6.8E-02 6
rs6906846 0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs7775397 0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs9272346 0.790 0.320 6 32636595 intron variant G/A snv 0.54 6