Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
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
rs2066363 0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 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
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs36001488 0.724 0.240 2 233276621 intron variant C/T snv 0.44 14
rs4869313 0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs6689858 0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs7042370 0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs7100025 0.724 0.240 10 37303610 intron variant G/A snv 0.68 14
rs72743477 0.724 0.240 15 67171953 intron variant A/G snv 0.17 14
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs77150043 0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14