Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9719620 0.807 0.080 7 131309621 non coding transcript exon variant T/A;C snv 7
rs939963 0.807 0.080 7 69122810 upstream gene variant G/C snv 0.67 7
rs9357047 0.807 0.080 6 9327323 intergenic variant T/A;C snv 7
rs9300169 0.807 0.080 12 26273738 non coding transcript exon variant A/G snv 0.55 7
rs9287638 0.807 0.080 2 238785990 downstream gene variant C/A snv 0.40 7
rs9282858 0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 16
rs8085664 0.807 0.080 18 45234191 intron variant C/A;T snv 7
rs7974900 0.807 0.080 12 26275744 intron variant T/A;C snv 7
rs79437808 0.807 0.080 8 108585572 intron variant C/T snv 1.3E-02 7
rs7801037 0.807 0.080 7 18857888 intron variant C/A;G;T snv 7
rs78003935 0.807 0.080 1 170372381 upstream gene variant T/A;G snv 0.25 7
rs77767830 0.807 0.080 8 108256167 intron variant A/T snv 2.5E-02 7
rs76972608 0.807 0.080 12 130078818 intergenic variant A/T snv 0.13 7
rs7680591 0.807 0.080 4 80276795 intron variant T/A snv 0.58 7
rs7642536 0.807 0.080 3 139313491 intron variant T/C snv 0.12 7
rs7542354 0.807 0.080 1 10980328 intron variant G/A snv 0.37 7
rs7534070 0.807 0.080 1 25171684 intergenic variant G/A;T snv 7
rs74333950 0.807 0.080 2 218881570 intron variant T/G snv 0.13 7
rs7349332 0.807 0.080 2 218891661 intron variant C/G;T snv 7
rs7177657 0.807 0.080 15 69749354 intron variant T/C snv 8.7E-02 7
rs71530654 0.807 0.080 7 18857365 intron variant A/G snv 0.43 7
rs71421546 0.807 0.080 2 176127129 intron variant C/A;T snv 7
rs7061504 0.807 0.080 X 68143959 intron variant A/G snv 0.23 7
rs6945541 0.807 0.080 7 69146973 intron variant C/T snv 0.68 7
rs68088846 0.807 0.080 21 34835870 intron variant G/A snv 0.27 7