Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
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
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs786204929 0.752 0.200 10 87933144 stop gained G/A;T snv 12
rs121909218 0.672 0.360 10 87933145 missense variant G/A snv 25
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147