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
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
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
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs3219489 0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs10877887 0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs4957014 0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs3756712 0.790 0.160 5 308981 non coding transcript exon variant A/C;T snv 10
rs1049216 0.790 0.200 4 184628935 3 prime UTR variant A/G snv 0.27 9
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs727088 0.790 0.400 18 69863203 3 prime UTR variant G/A snv 0.47 8
rs3087386 0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs9298814 0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7
rs4705343 0.790 0.240 5 149428518 non coding transcript exon variant T/C snv 0.14 7
rs4282438 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 6
rs13117307 0.827 0.080 4 55885574 intron variant C/T snv 0.21 6