Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs9272346 0.790 0.320 6 32636595 intron variant G/A snv 0.54 6
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 5