Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 7
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 5
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 4
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 3
rs2157719 0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 3
rs907611 0.882 0.160 11 1852842 upstream gene variant G/A snv 0.26 3
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 3
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 3
rs11892031 0.882 0.120 2 233656637 intron variant A/C;T snv 3
rs710521 0.851 0.200 3 189928144 intergenic variant T/C snv 0.24 2
rs9642880 0.776 0.240 8 127705823 intron variant G/A;T snv 2
rs1014971 0.882 0.120 22 38936618 regulatory region variant C/T snv 0.55 1
rs2204008 1.000 0.120 12 38045401 intergenic variant C/A;T snv 1
rs62185668 0.925 0.120 20 10981287 intron variant C/A snv 0.19 1
rs8102137 0.882 0.120 19 29805946 regulatory region variant T/C snv 0.24 1
rs1046778 0.851 0.160 10 102901727 3 prime UTR variant T/C snv 0.30 1
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 1
rs10094872 0.882 0.200 8 127707639 intron variant A/T snv 0.33 1
rs4510656 0.925 0.120 6 20766466 intron variant C/A snv 0.39 1
rs7747724 0.925 0.120 6 20751084 intron variant T/C snv 0.41 1