Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3219218
UNG
0.851 0.120 12 109100430 intron variant A/G snv 1.9E-02 4
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs9610 0.882 0.240 11 118001371 3 prime UTR variant G/A;T snv 0.51 4
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs853360 1.000 0.080 6 14134361 intron variant T/C snv 0.74 1
rs4705343 0.790 0.240 5 149428518 non coding transcript exon variant T/C snv 0.14 7
rs3181224 1.000 0.080 5 159313842 intron variant A/G snv 0.10 1
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs750553272 0.851 0.080 2 177230898 missense variant G/A snv 1.2E-05 7.0E-06 4
rs3729679 1.000 0.080 3 179204642 intron variant A/G snv 0.58 1
rs12494623 1.000 0.080 3 179214763 intron variant C/G;T snv 1
rs1049216 0.790 0.200 4 184628935 3 prime UTR variant A/G snv 0.27 9
rs9298814 0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs3024656 1.000 0.080 16 27358288 intron variant G/A snv 0.20 1
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
rs4282438 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 6
rs9277952 0.851 0.080 6 33236497 upstream gene variant G/A snv 0.10 4
rs3748079 0.925 0.160 6 33620370 5 prime UTR variant C/T snv 0.18 2
rs2229634 0.851 0.240 6 33670403 synonymous variant C/A;T snv 4.0E-06; 0.33 4
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs16997517 0.925 0.200 22 36937894 missense variant C/T snv 2.6E-02 4.7E-02 2