Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587782596 0.807 0.200 17 7675071 missense variant G/A;T snv 7
rs1214285376 0.776 0.200 19 43543490 missense variant G/T snv 4.0E-06 8
rs17021918 0.776 0.240 4 94641726 intron variant C/T snv 0.30 8
rs2180314 0.776 0.200 6 52752933 missense variant C/G snv 0.60 0.52 8
rs2303425 0.790 0.120 2 47403074 5 prime UTR variant T/C snv 0.10 8
rs3136820 0.776 0.200 14 20456995 missense variant T/A;C;G snv 8
rs3817198 0.790 0.280 11 1887776 intron variant T/C snv 0.26 8
rs587782705 0.807 0.280 17 7675157 missense variant G/A snv 8.0E-06 8
rs62514004 0.790 0.240 8 133190246 upstream gene variant A/G snv 0.28 8
rs664143 0.807 0.160 11 108354934 3 prime UTR variant A/G;T snv 8
rs664677
ATM
0.807 0.160 11 108272455 intron variant C/A;T snv 0.65 8
rs751763046 0.790 0.200 1 241885375 missense variant T/C snv 4.0E-06 8
rs8102476 0.776 0.240 19 38244973 intron variant C/T snv 0.40 8
rs1635498 0.807 0.160 1 241881973 missense variant C/A;G;T snv 0.96 9
rs1776148 0.807 0.160 1 241879243 missense variant A/G snv 0.66 0.66 9
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9
rs2602141 0.790 0.120 15 43432448 missense variant T/G snv 0.36 0.47 9
rs45446698 0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 9
rs7086803 0.763 0.160 10 112738717 intron variant G/A snv 0.20 9
rs7904519 0.763 0.240 10 113014168 intron variant A/G snv 0.55 9
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs1204382931 0.790 0.160 2 38075270 missense variant A/C snv 4.3E-06 10
rs3136797 0.827 0.120 8 42369287 missense variant C/G snv 1.1E-02 1.1E-02 10
rs3731239 0.763 0.240 9 21974219 intron variant A/G snv 0.26 10
rs4809957 0.763 0.240 20 54154632 3 prime UTR variant A/G snv 0.29 10