Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs11082304 18 23141009 intron variant G/C;T snv 6
rs34651 1.000 0.040 5 72848178 non coding transcript exon variant C/T snv 0.94 5
rs2287922 19 48728969 missense variant G/A snv 0.37 0.37 3