Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1689510 0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs11741255 0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs4625 0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
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
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs36001488 0.724 0.240 2 233276621 intron variant C/T snv 0.44 14
rs12928404 0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs602662 0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 15
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs7042370 0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs7100025 0.724 0.240 10 37303610 intron variant G/A snv 0.68 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
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34