Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11544484 0.882 0.120 8 143324535 missense variant C/T snv 0.26 0.33 3
rs12203582 0.827 0.120 6 52240759 intron variant G/A;T snv 7
rs12443621 0.807 0.120 16 52514125 intron variant A/G snv 0.48 6
rs139029625 0.827 0.120 19 41010006 missense variant G/A;C;T snv 2.8E-05; 4.5E-04; 8.0E-06 5
rs1408630981 0.827 0.120 7 55205492 missense variant C/G snv 4.0E-06 5
rs1800264
DMD
0.827 0.120 X 32699141 missense variant A/C;G snv 5.5E-06; 8.3E-03 5
rs1805076 0.851 0.120 11 111764842 missense variant C/T snv 6.5E-03 7.0E-03 7
rs1805388 0.790 0.120 13 108211243 missense variant G/A snv 0.18 0.16 11
rs1864182 0.827 0.120 5 82253421 missense variant C/A;G snv 0.59 0.47 6
rs2303425 0.790 0.120 2 47403074 5 prime UTR variant T/C snv 0.10 8
rs2602141 0.790 0.120 15 43432448 missense variant T/G snv 0.36 0.47 9
rs3104746 0.790 0.120 16 52567188 intron variant T/A snv 8.6E-02 7
rs3134615 0.827 0.120 1 39896394 3 prime UTR variant C/A snv 0.17 5
rs3136797 0.827 0.120 8 42369287 missense variant C/G snv 1.1E-02 1.1E-02 10
rs34662244 0.925 0.120 6 28106103 intron variant G/A snv 5.0E-02 2
rs375275361 0.827 0.120 17 7675054 missense variant A/G;T snv 1.2E-05; 4.0E-06 5
rs3816358 0.827 0.120 11 13369925 intron variant C/A;T snv 5
rs3816360 0.807 0.120 11 13346203 intron variant T/C snv 0.58 6
rs3842530 0.827 0.120 1 209432292 non coding transcript exon variant GCAGCAGCAGCAGCAGCAGCAGCAGCA/-;GCA;GCAGCA;GCAGCAGCA;GCAGCAGCAGCA;GCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA;GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA delins 5
rs4246742 0.827 0.120 5 1267241 intron variant T/A snv 0.23 5
rs45446698 0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 9
rs5744533 0.807 0.120 5 75510279 intron variant C/A;T snv 6
rs624366
ATM
0.827 0.120 11 108283370 intron variant G/C snv 0.52 6
rs6413432 0.827 0.120 10 133535040 intron variant T/A snv 9.9E-02 5
rs757163626 0.827 0.120 22 19962726 missense variant C/T snv 1.6E-05 7.0E-06 5