Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1520220 0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs17728461 0.776 0.120 22 30202563 intron variant C/G snv 0.25 9
rs4648068 0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs6713088 0.763 0.200 2 54118332 intron variant C/G snv 0.48 9
rs11896604 0.776 0.200 2 54252062 intron variant C/A;G;T snv 8
rs4958847 0.807 0.120 5 150860025 intron variant G/A snv 0.25 8
rs10052657 0.807 0.120 5 59111944 intron variant C/A snv 0.17 7
rs10074991 0.851 0.120 5 40790449 intron variant G/A snv 0.31 7
rs10499563 0.807 0.120 7 22720869 intron variant T/C snv 0.21 7
rs13361707 0.882 0.120 5 40791782 intron variant C/T snv 0.31 7
rs17045754 0.790 0.280 2 54269620 intron variant G/A;C snv 7
rs2808668
XPA
0.851 0.120 9 97690153 intron variant C/G;T snv 7
rs2976391
PSCA ; JRK
0.790 0.160 8 142681306 intron variant C/A;G snv 0.42; 2.5E-04 7
rs3790843 0.827 0.160 1 200041696 intron variant C/T snv 0.29 7
rs79071878 0.827 0.240 5 132680652 intron variant ATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGACGATGGTGGCGTGGACAGAATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGATGATGGTGGCGTGGACAGAAT/- del 7
rs9297976
JRK ; PSCA
0.790 0.160 8 142670817 intron variant T/C;G snv 7
rs9841504 0.827 0.120 3 114643917 intron variant C/G;T snv 7
rs115797771 0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs12108497 0.851 0.080 4 184650403 intron variant C/G;T snv 6
rs12229892 0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs12304647 0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs1562430 0.807 0.160 8 127375606 intron variant T/C snv 0.41 6
rs1760893 0.807 0.080 14 20412501 intron variant C/A snv 0.89 6
rs6733868 0.851 0.120 2 25276998 intron variant C/G snv 0.50 6
rs828907 0.827 0.160 2 216108009 intron variant G/T snv 0.37 6