Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
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
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
rs114846446 0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11580078 0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs11741255 0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs1250563 0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 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
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
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
rs77150043 0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs10174238 0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs6584283 0.776 0.080 10 99530544 intron variant T/C snv 0.56 12