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 25
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 5
rs4410790 0.882 0.160 7 17244953 intron variant T/C snv 0.54 5