Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1131691041
rs1131691041
3 17 7676271 frameshift variant -/A delins 0.010 1.000 1 2017 2017
dbSNP: rs12498609
rs12498609
1 4 105234028 missense variant C/G;T snv 6.3E-02; 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs228593
rs228593
ATM
1 11 108270407 intron variant G/A snv 0.27 0.010 1.000 1 2016 2016
dbSNP: rs3746609
rs3746609
1 20 32434666 missense variant G/A snv 1.9E-02; 4.4E-06 7.4E-03 0.010 1.000 1 2019 2019
dbSNP: rs72661120
rs72661120
1 17 7673717 synonymous variant T/C snv 2.7E-04 7.0E-05 0.010 1.000 1 2001 2001
dbSNP: rs752492487
rs752492487
1 15 40718847 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs775743629
rs775743629
1 6 162262719 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs781517199
rs781517199
1 20 50082788 missense variant C/G snv 4.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs893810317
rs893810317
1 X 48793910 missense variant C/T snv 0.010 1.000 1 2014 2014
dbSNP: rs1178981336
rs1178981336
2 1.000 0.040 9 113424228 frameshift variant -/G delins 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs138817062
rs138817062
PML
4 0.882 0.040 15 74044940 missense variant C/T snv 4.0E-05 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs142883642
rs142883642
2 1.000 0.040 2 208248486 missense variant T/C snv 3.6E-05 2.1E-05 0.010 1.000 1 2010 2010
dbSNP: rs767232094
rs767232094
2 1.000 0.040 16 55484157 synonymous variant C/T snv 8.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs387906631
rs387906631
6 0.882 0.080 3 128481901 missense variant G/A snv 0.820 1.000 2 2011 2012
dbSNP: rs751689316
rs751689316
4 0.925 0.080 3 169131510 missense variant C/T snv 1.2E-05 0.020 1.000 2 2008 2013
dbSNP: rs1408538785
rs1408538785
6 0.827 0.080 6 38761760 missense variant A/G snv 7.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs2228529
rs2228529
4 0.925 0.080 10 49459059 missense variant T/C snv 0.22 0.19 0.010 1.000 1 2019 2019
dbSNP: rs4135113
rs4135113
TDG
5 0.925 0.080 12 103982915 missense variant G/A;C;T snv 4.7E-02 0.010 1.000 1 2019 2019
dbSNP: rs587779821
rs587779821
ATM
2 1.000 0.080 11 108259059 missense variant A/G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs762622506
rs762622506
3 0.925 0.080 X 40074459 missense variant C/A;T snv 6.1E-06 0.010 1.000 1 2018 2018
dbSNP: rs867679539
rs867679539
3 0.925 0.080 X 130013883 missense variant A/C snv 0.010 1.000 1 2018 2018
dbSNP: rs869312828
rs869312828
7 0.807 0.080 5 177512369 missense variant C/T snv 0.010 1.000 1 2017 2017
dbSNP: rs121913488
rs121913488
7 0.807 0.120 13 28018505 missense variant C/A;G;T snv 0.010 1.000 1 2004 2004
dbSNP: rs1805388
rs1805388
11 0.790 0.120 13 108211243 missense variant G/A snv 0.18 0.16 0.010 1.000 1 2016 2016
dbSNP: rs3835
rs3835
4 0.882 0.120 2 216201914 intron variant G/A snv 0.21 0.010 1.000 1 2015 2015