Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9272346 0.790 0.320 6 32636595 intron variant G/A snv 0.54 6
rs2076530 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 5
rs3806156 0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 5
rs9268645 0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 4
rs2239800 0.882 0.280 6 32745490 intron variant A/G snv 0.11 3
rs3101942 0.882 0.200 6 32902280 intergenic variant G/A;C snv 3
rs6903130 0.882 0.200 6 32764433 upstream gene variant G/A snv 0.53 3
rs415929 0.925 0.200 6 32221255 synonymous variant T/C snv 0.31 0.29 2