Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113577745 1.000 0.080 2 9995553 intron variant C/G snv 8.8E-02 1
rs45446698 0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 3
rs11298677 1.000 0.080 3 99682866 intron variant G/- delins 0.60 1
rs776746 0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 1
rs79518236 1.000 0.080 7 98397243 intron variant CT/- delins 0.24 1
rs17356907 0.925 0.080 12 95633983 intron variant A/G snv 0.28 2
rs757158 0.851 0.240 7 95326216 upstream gene variant C/T snv 0.58 1
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 1
rs10269006 1.000 0.080 7 94758031 intergenic variant G/T snv 0.32 1
rs111307654 1.000 0.080 7 94655777 intron variant -/AA;AAA;AAAA delins 1
rs17021918 0.776 0.240 4 94641726 intron variant C/T snv 0.30 1
rs17268829 1.000 0.080 7 94484487 intergenic variant T/C snv 0.22 1
rs1858826 1.000 0.080 7 93719703 intron variant C/T snv 0.90 3
rs140936696 1.000 0.080 10 93532431 downstream gene variant AAAAAAA/-;AA;AAA;AAAA;AAAAA;AAAAAA;AAAAAAAA;AAAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAA delins 1
rs73419340 1.000 0.080 7 93388705 intergenic variant G/A snv 7.7E-02 1
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 1
rs11627032 1.000 0.080 14 92637727 intron variant T/C snv 0.22 1
rs2771267 1.000 0.080 10 92388574 intergenic variant A/T snv 0.52 1
rs369328859 1.000 0.080 7 92344194 intron variant TTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT delins 1
rs35522438 1.000 0.080 7 92243558 intron variant -/T delins 0.40 1
rs35417517 1.000 0.080 7 92143417 intron variant G/- delins 0.44 1
rs10644111 1.000 0.080 7 92022864 protein altering variant -/AAC delins 0.39 0.46 1
rs6964587 0.851 0.120 7 92001306 missense variant G/T snv 0.38 0.42 1
rs421379 0.925 0.080 5 91979496 intergenic variant T/C snv 0.75 1
rs9884765 1.000 0.080 4 91717049 intergenic variant T/A;C snv 1