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
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs3219218
UNG
0.851 0.120 12 109100430 intron variant A/G snv 1.9E-02 4