Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2479409 1.000 0.040 1 55038977 upstream gene variant G/A snv 0.66 4
rs7025486 0.851 0.040 9 121660124 intron variant G/A snv 0.28 4
rs12133641 0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs12695895 0.925 0.040 3 148725481 intron variant C/T snv 0.31 3
rs4916251 0.882 0.040 1 172377256 intron variant T/A snv 0.70 3
rs2234681 1.000 0.040 20 46008773 upstream gene variant ACACACACACACACACACACACAC/-;AC;ACAC;ACACAC;ACACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACAC;ACACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC;ACACACACACACACACACACACACAC;ACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACACAC delins 2
rs3827066 0.925 0.040 20 45957384 intron variant C/T snv 0.12 2
rs1036095 1.000 0.040 3 30620836 intron variant C/G snv 0.72 1
rs1057518075 1.000 0.040 2 188995061 stop gained C/T snv 1
rs10758278 1.000 0.040 9 34825306 intron variant G/A snv 0.53 1
rs10985349 1.000 0.040 9 121662964 intron variant C/T snv 0.17 1
rs13382862 1.000 0.040 2 20682689 upstream gene variant A/G;T snv 0.59 1
rs1385526 1.000 0.040 12 57138966 intron variant G/C snv 0.26 1
rs1418184396 1.000 0.040 17 1776722 missense variant C/T snv 4.0E-06 1
rs1419338705
ELN
1.000 0.040 7 74048163 missense variant C/T snv 7.0E-06 1
rs1795061 1.000 0.040 1 214235937 intergenic variant T/C;G snv 1
rs2070863 1.000 0.040 17 1745208 missense variant C/G;T snv 0.24 1
rs2306691 1.000 0.040 12 57145019 missense variant A/G snv 2.0E-05 2.1E-05 1
rs2652106 1.000 0.040 5 83498217 intron variant G/T snv 0.39 1
rs2836411
ERG
1.000 0.040 21 38447907 intron variant C/A;T snv 1
rs3781590 1.000 0.040 11 68391684 intron variant G/A snv 0.35 1
rs58749629 1.000 0.040 20 45942678 intron variant G/A;T snv 0.13 1
rs6674171 1.000 0.040 1 154519207 intron variant A/G;T snv 0.19 1
rs766407419 1.000 0.040 17 1745008 missense variant T/C snv 8.0E-06 1.4E-05 1
rs767169659 1.000 0.040 3 123733800 missense variant G/A snv 1.2E-05 1