Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs483143 0.925 0.080 6 27878966 intergenic variant G/C snv 0.13 2
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs9980603 0.925 0.080 21 40514656 intron variant T/C snv 0.40 2
rs8067056 0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5