Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2240335 1.000 0.120 1 17348042 synonymous variant C/A snv 0.39 0.37 1
rs2240336 1.000 0.120 1 17347907 intron variant C/T snv 0.43 0.45 1
rs2240339 1.000 0.120 1 17347613 intron variant C/T snv 0.36 1
rs2301888 1.000 0.120 1 17346235 intron variant G/A snv 0.31 1