Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 6
rs2050392 0.827 0.120 10 30402574 downstream gene variant G/A snv 0.45 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2497318 0.827 0.120 10 92672243 upstream gene variant C/A;T snv 6
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs4703855 0.827 0.120 5 72398072 regulatory region variant C/T snv 0.24 6
rs4848306 0.851 0.120 2 112840530 non coding transcript exon variant G/A snv 0.39 6
rs4917129 0.807 0.240 7 50283578 intergenic variant T/C snv 0.51 6
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 6
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 6
rs71559680 0.827 0.120 6 21430497 intergenic variant TAG/CAT mnv 6
rs7426056 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 6
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 6
rs9687958 0.827 0.120 5 40496321 intron variant G/T snv 0.60 6
rs9889296 0.827 0.120 17 34243528 intergenic variant G/A snv 0.33 6
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5
rs10750899 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 5
rs10800314 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 5
rs111305875 0.827 0.120 6 167098098 intron variant T/G snv 3.0E-02 5
rs11190133 0.827 0.120 10 99518968 intergenic variant C/T snv 0.26 5
rs11306716 0.827 0.120 2 203843041 intergenic variant T/-;TT delins 5