Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs2234767 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs10821936 0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs7089424 0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs41293463 0.790 0.280 17 43051071 missense variant A/C;T snv 1.2E-05 9
rs1057519753 0.763 0.120 1 64846664 missense variant C/A snv 9
rs11191439 0.851 0.120 10 102878966 missense variant T/A;C snv 9.2E-02 6
rs10748835 0.827 0.160 10 102900499 non coding transcript exon variant G/A snv 0.41 5
rs7560488 0.851 0.160 2 25345952 upstream gene variant T/C snv 0.40 4
rs7073837 0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 4
rs2393726 0.925 0.040 10 62094648 3 prime UTR variant A/G snv 3.9E-02 2
rs6415872 0.925 0.040 10 61900930 upstream gene variant G/A snv 0.51 2
rs3740390 0.925 0.080 10 102878723 intron variant C/T snv 9.2E-02 2
rs11191453 1.000 0.040 10 102900095 intron variant T/C snv 9.0E-02 1