Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11580078 0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs2066363 0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs6689858 0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs114846446 0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs36001488 0.724 0.240 2 233276621 intron variant C/T snv 0.44 14
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs4625 0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
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
rs11741255 0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs4869313 0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs10988542 0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763 0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs7042370 0.724 0.240 9 12785074 intron variant T/C snv 0.58 14