Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs71624119 0.776 0.200 5 56144903 intron variant G/A snv 0.17 7
rs1250550 0.851 0.240 10 79300560 intron variant C/A snv 0.27 5
rs8070463 0.925 0.120 17 47691470 upstream gene variant T/C snv 0.54 2