Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13428812 0.827 0.120 2 25269598 intron variant A/G snv 0.31 8
rs4958847 0.807 0.120 5 150860025 intron variant G/A snv 0.25 8
rs7758229 0.732 0.120 6 160419220 intron variant G/A;T snv 8
rs10499563 0.807 0.120 7 22720869 intron variant T/C snv 0.21 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
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
rs12304647 0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs13361707 0.882 0.120 5 40791782 intron variant C/T snv 0.31 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
rs830083 0.807 0.120 11 47232500 intron variant G/A;C;T snv 6
rs9841504 0.827 0.120 3 114643917 intron variant C/G;T snv 6
rs10074991 0.851 0.120 5 40790449 intron variant G/A snv 0.31 5
rs10509670 0.851 0.080 10 94308190 intron variant A/G snv 0.30 5
rs10739971 0.882 0.080 9 94175398 intron variant G/A;C snv 5
rs11536878 0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02 5
rs1864169 0.851 0.200 14 81203689 intron variant G/T snv 0.78 5