Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs16875288 0.851 0.040 5 5297087 intron variant A/T snv 0.22 4
rs17158930 0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs16935279 0.851 0.040 8 68961217 intron variant T/C snv 1.9E-02 4
rs10968749 0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs9862857 0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs11829119 0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs2302045 0.851 0.040 2 241081801 splice region variant G/A snv 7.6E-02 1.0E-01 4
rs17673138 0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4
rs144733372 0.882 0.120 17 45486856 intron variant T/G snv 4
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs17211233 0.882 0.040 5 81072944 intron variant T/A;C snv 4
rs17790731 0.851 0.040 5 95647825 5 prime UTR variant C/T snv 4.9E-02 4
rs55945116 0.882 0.040 15 84676882 intron variant G/C snv 0.26 4
rs139438618 0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 4
rs10405744 0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs853679 0.851 0.160 6 28329086 intron variant C/A snv 0.20 4
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-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