Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs602662 0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 15
rs1689510 0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs17466626 0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs17885785 0.724 0.240 11 2146620 non coding transcript exon variant C/T snv 0.14 14
rs117372389 0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs4625 0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs12928404 0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14