Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs2240308 0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs1219648 0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs1800054
ATM
0.827 0.080 11 108227849 missense variant C/G;T snv 7.1E-03 7
rs987525 0.807 0.160 8 128933908 intron variant C/A snv 0.31 7