Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs31490 0.776 0.280 5 1344343 splice region variant G/A;T snv 0.37; 8.0E-06 2
rs757978 0.851 0.200 2 241431686 missense variant C/A;T snv 4.1E-06; 9.3E-02 2
rs11668878 0.925 0.200 19 46765116 intron variant G/T snv 5.1E-02 2
rs1050976 0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37 2
rs391525 0.882 0.200 16 85910833 intron variant A/G;T snv 0.35 2
rs11083846 0.882 0.200 19 46704397 splice region variant G/A snv 0.17 0.16 2
rs3803800 0.807 0.240 17 7559652 missense variant A/G snv 0.70 0.64 2
rs13069553 0.851 0.200 3 169790484 upstream gene variant A/G snv 0.21 1
rs1359742 0.925 0.120 9 22336997 intergenic variant G/C;T snv 1
rs1679013 0.882 0.160 9 22206988 intron variant C/A;T snv 0.43 1
rs2511714 0.925 0.120 8 102566646 regulatory region variant T/G snv 0.41 1
rs35748167 1.000 0.120 18 60370200 intron variant G/C;T snv 1
rs391023 0.925 0.120 16 85894208 upstream gene variant C/T snv 0.48 1
rs4368253 0.925 0.120 18 59955055 TF binding site variant T/A;C snv 1
rs674313 0.925 0.120 6 32610305 intergenic variant C/T snv 0.29 1
rs7944004 0.925 0.120 11 2289922 intergenic variant T/G snv 0.48 1
rs8024033 0.925 0.120 15 40111456 upstream gene variant C/G snv 0.50 1
rs13401811 0.925 0.120 2 110858527 intron variant G/A snv 0.19 1
rs1439287 0.925 0.120 2 111114320 non coding transcript exon variant G/A snv 0.42 1
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 1
rs4987852 0.925 0.120 18 63126688 3 prime UTR variant T/C snv 5.1E-02 1
rs4987855 0.925 0.120 18 63126316 3 prime UTR variant C/T snv 5.9E-02 1
rs4987856 0.925 0.120 18 63126261 3 prime UTR variant C/T snv 6.0E-02 1
rs6858698 0.925 0.120 4 113762688 upstream gene variant G/C snv 0.20 1
rs2466032 1.000 0.120 8 127197575 non coding transcript exon variant T/C snv 0.23 1