Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1420101 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 3
rs9807989 1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 2
rs5833013 2 102352407 intron variant -/TA delins 2
rs6543119 2 102346612 intron variant A/T snv 0.36 1