Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2239705 1.000 0.120 6 31545625 intron variant G/A snv 0.18 0.16 1
rs2230365 0.925 0.160 6 31557671 synonymous variant C/T snv 0.16 0.13 1
rs6929796 1.000 0.120 6 31554892 intron variant G/A snv 0.22 1
rs2523503 1.000 0.120 6 31545782 non coding transcript exon variant C/A snv 0.15 1