Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs536562413 0.732 0.240 2 47799934 missense variant A/G snv 1.2E-05 7.0E-06 15
rs13428812 0.827 0.120 2 25269598 intron variant A/G snv 0.31 9
rs6733868 0.851 0.120 2 25276998 intron variant C/G snv 0.50 6