Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10233018 0.925 0.040 7 117883655 non coding transcript exon variant A/G snv 0.53 2
rs10485715 0.925 0.040 20 7279278 intergenic variant T/C snv 5.5E-02 2
rs10809520 0.925 0.040 9 11557797 intergenic variant C/T snv 0.28 2
rs10884216 0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 2
rs11082011 0.925 0.040 18 37565159 intron variant C/T snv 0.53 3
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs11155372 0.925 0.040 6 144698602 intron variant G/C;T snv 3
rs112106319 0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs11591827 0.925 0.040 10 81128126 intergenic variant G/A snv 8.4E-02 3
rs116609693 0.925 0.040 9 92811394 intron variant C/T snv 6.1E-02 2
rs11728985 0.925 0.040 4 129115280 3 prime UTR variant C/T snv 0.12 3
rs11924809 0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs11990063 0.925 0.040 8 10307685 intron variant C/A;T snv 3
rs12555870 0.925 0.040 9 23347726 intron variant A/G snv 0.36 3
rs1352618632 0.925 0.040 13 33112802 missense variant T/C snv 4.0E-06 2
rs1401635 0.925 0.040 11 27672444 intron variant C/G snv 0.73 4
rs1411216 0.925 0.040 9 24520196 intergenic variant A/G snv 0.73 3
rs142484554 0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs142641502 0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs143405544 0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 3
rs143934587 0.925 0.040 20 19165806 intergenic variant G/A snv 9.1E-03 3
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs1690818 0.925 0.040 11 99625823 intron variant C/T snv 0.61 2
rs17156280 0.925 0.040 7 82414674 intron variant T/C snv 3.4E-02 2