Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs779162432 0.790 0.080 2 169637315 missense variant A/G snv 4.1E-06 7
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs743572 0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs3824260 0.742 0.160 8 58500631 upstream gene variant A/G;T snv 11
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs2303426 0.790 0.080 2 47403411 intron variant C/A;G;T snv 1.9E-05; 0.47 8
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
rs20575 0.645 0.440 8 23201811 missense variant C/G snv 0.54 0.44 29
rs2072668 0.732 0.280 3 9756456 intron variant C/G snv 0.28 0.24 14
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs4595552 0.790 0.080 11 125865825 intergenic variant C/G;T snv 7
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36