Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs874040 0.925 0.160 4 26106575 downstream gene variant G/C snv 0.29 4
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs4819388 0.790 0.240 21 44227538 3 prime UTR variant T/C snv 5
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 5
rs212389 0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 3
rs4750316 0.882 0.160 10 6351298 non coding transcript exon variant C/G;T snv 4
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs3748816 0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs13314993 0.882 0.200 3 32973977 regulatory region variant G/C;T snv 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs10806425 0.851 0.280 6 90216893 intron variant C/A snv 0.33 5
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs11676922 0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs11712165 0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs1250552 0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs12928822 0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 7