Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs56848936 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 11
rs3753584 0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs1443465532 0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6
rs17878467 0.925 0.080 17 78214076 upstream gene variant C/G;T snv 6
rs5273 0.827 0.080 1 186674636 missense variant A/C;G snv 4.0E-06; 7.6E-03 1.4E-02 6
rs60745952 0.925 0.080 4 148827842 intron variant T/C snv 0.13 6
rs6854845 0.827 0.080 4 74821455 intergenic variant G/T snv 0.13 6
rs1289280947 0.851 0.080 9 21974571 missense variant C/T snv 4.0E-06 5
rs2853668 0.882 0.080 5 1299910 upstream gene variant G/T snv 0.33 5
rs35301225 0.882 0.080 1 9151743 mature miRNA variant C/A;T snv 5
rs3775292 0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82 5
rs4135113
TDG
0.925 0.080 12 103982915 missense variant G/A;C;T snv 4.7E-02 5
rs9365723 0.827 0.080 6 158014540 intron variant A/C;G snv 0.56 5
rs10222633 0.925 0.080 3 122258079 intron variant G/A snv 0.45 4
rs10934578 0.925 0.080 3 122258435 intron variant G/T snv 0.30 4
rs12591359 0.925 0.080 15 51247171 intron variant G/A snv 0.41 4
rs2737 0.851 0.080 17 47981705 missense variant T/C snv 0.25 0.19 4
rs2770150 0.925 0.080 9 117700861 upstream gene variant A/G snv 0.22 4
rs3804513 0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02 4
rs6588147 0.851 0.080 1 65469811 intron variant G/A snv 0.70 4
rs756363791 0.882 0.080 3 9756823 missense variant G/A snv 2.0E-05 4
rs7987649 0.925 0.080 13 28320278 intron variant A/G snv 0.35 4