Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10174238 0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs10954214 0.851 0.160 7 128949579 3 prime UTR variant C/T snv 0.64 4
rs11066301 0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs11085725 0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs112846137 0.851 0.160 3 160595133 intergenic variant G/T snv 5.3E-02 4
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 3
rs1217393 0.851 0.160 1 113891324 intron variant G/A snv 0.42 4
rs12531711 0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs13101828 0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs13238352 0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 4
rs13389408 0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02 4
rs193107685 0.851 0.160 7 74123572 downstream gene variant T/C snv 1.0E-02 4
rs2283790 0.882 0.120 22 21602364 intron variant A/G snv 0.21 3
rs2422345 0.851 0.160 1 173368608 upstream gene variant G/A snv 0.63 4
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 4
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs4810485 0.732 0.480 20 46119308 intron variant T/A;G snv 3
rs4921283 0.925 0.120 5 160443604 intron variant G/A snv 0.52 2
rs4958880 0.851 0.160 5 151058916 intron variant C/A;G snv 4
rs5029924 0.851 0.200 6 137866361 intron variant C/T snv 0.13 2
rs5754467 0.851 0.160 22 21630805 upstream gene variant A/G;T snv 4