Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs2247056 0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs477515 0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 7
rs2076530 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 5
rs2239804 0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs2395157 0.827 0.240 6 32380368 intron variant A/G snv 0.24 5
rs2395182 0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76 5
rs3817963 0.776 0.360 6 32400310 intron variant T/C snv 0.25 5
rs3793126 0.882 0.240 6 32403842 intron variant A/G snv 0.24 3
rs412657 0.882 0.240 6 32243308 intergenic variant T/C;G snv 3
rs6910071 0.790 0.320 6 32315077 intron variant A/G snv 0.14 3