Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs228591
ATM
11 108226606 5 prime UTR variant A/G snv 0.54 1
rs624366
ATM
0.827 0.120 11 108283370 intron variant G/C snv 0.52 1
rs645485
ATM
11 108298136 intron variant A/G snv 0.54 1
rs227041 11 108352074 intron variant C/A snv 0.52 1
rs227073 11 108341965 intron variant G/A;C;T snv 1
rs419716 11 108350372 intron variant A/C;T snv 1
rs11212617 0.827 0.200 11 108412434 intron variant C/A snv 0.49 1
rs227077 11 108382525 intron variant C/A;T snv 1
rs573890 11 108380636 intron variant C/G;T snv 0.53 1
rs7931930 11 108397559 intron variant G/T snv 0.49 1
rs12787445 11 108163397 intron variant A/G snv 0.35 1
rs183460 11 108219983 intron variant A/C;T snv 1
rs609557 11 108213786 intron variant G/A;T snv 1
rs6589007 11 108169377 intron variant A/G snv 0.55 1