Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs6903608 0.742 0.400 6 32460508 intron variant C/G;T snv 5
rs9268831 0.851 0.280 6 32459971 non coding transcript exon variant C/T snv 0.54 0.51 3