Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11394256 10 45461799 non coding transcript exon variant -/A delins 0.23 1
rs35762459 11 8823106 intron variant -/A delins 0.46 1
rs36064799 17 35553480 non coding transcript exon variant -/A delins 4.5E-02 7.5E-02 1
rs5781151 1 219912854 intron variant -/A;AA delins 1
rs3053386 6 2488103 intron variant -/AA delins 1
rs10649609 2 164696196 non coding transcript exon variant -/AATAA;AGTAA delins 1
rs140297755 9 74364686 intergenic variant -/ACA delins 0.31 1
rs148280884 6 30159781 intron variant -/AT ins 2.7E-02 1
rs11438927 12 120746070 intron variant -/C ins 0.42 1
rs57675369 5 95826714 upstream gene variant -/G ins 0.14 1
rs147324647 6 132499140 intron variant -/GT;T ins 1
rs113700287 3 24293020 intron variant -/GTT delins 4
rs34978289 6 2504388 intron variant -/T ins 0.53 1
rs35237755 1 247868934 intron variant -/T delins 1.0E-01 1
rs11429307 5 56561198 intron variant -/T;TT delins 1
rs397778518 3 172081346 intron variant -/T;TT delins 0.49 1
rs68021656 2 111165509 3 prime UTR variant -/T;TT delins 1
rs139300217 10 45524767 intron variant -/TA delins 1.4E-02 1
rs397826789 1 23783400 intron variant -/TA;TACACACATATATGTGTATATATACATATATACACATATATATA;TACACATATATATGCGTATATATACATATATACGCATATATATA;TACACATATATGTGTATATATACATATATACGCATATATATA;TATA delins 0.63 1
rs111326718 10 103011454 intron variant -/TAAAA delins 0.40 1
rs71378803 2 86779042 downstream gene variant -/TC delins 0.62 1
rs111373852 6 6679939 downstream gene variant -/TTAG delins 0.54 1
rs141119689 1 155301643 upstream gene variant A/- del 4.4E-02 1
rs10716881 12 56644387 intron variant A/-;AA delins 0.42 1
rs34756862 9 34057211 intergenic variant A/-;AA delins 1