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: rs1564045331
rs1564045331
XPA
35 0.716 0.320 9 97687208 inframe deletion ATTCTT/- delins 0.700 0
dbSNP: rs778543124
rs778543124
XPA
35 0.716 0.320 9 97675476 frameshift variant AGTCTTACGGTACA/- delins 6.8E-05 6.3E-05 0.700 0
dbSNP: rs777593389
rs777593389
3 1.000 0.320 8 99156693 stop gained C/T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs34757931
rs34757931
26 0.742 0.360 11 119081189 missense variant T/G snv 1.2E-04 5.6E-05 0.700 0
dbSNP: rs1555582065
rs1555582065
13 0.827 0.160 17 44212851 missense variant C/T snv 0.700 0
dbSNP: rs386834034
rs386834034
9 0.790 0.240 1 46194853 stop gained G/A;T snv 2.0E-05 0.700 1.000 1 2016 2016
dbSNP: rs184953805
rs184953805
8 0.882 0.200 3 48467284 stop gained G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs78300695
rs78300695
8 0.882 0.200 3 48466711 frameshift variant -/G delins 2.1E-05 0.700 1.000 1 2016 2016
dbSNP: rs864309505
rs864309505
10 0.807 0.200 11 6615220 missense variant T/G snv 0.700 0
dbSNP: rs878855331
rs878855331
5 0.925 0.120 11 6617319 splice donor variant AAGGCCTGTGGAAGCTGGTAGGGATGTGGGGACC/- delins 0.700 0
dbSNP: rs1554558365
rs1554558365
4 0.925 0.120 8 93804851 inframe insertion -/TATGAA delins 0.700 0
dbSNP: rs765468645
rs765468645
5 0.882 0.160 8 93765413 stop gained C/T snv 8.0E-06 2.1E-05 0.700 0
dbSNP: rs1569146993
rs1569146993
5 0.851 0.320 22 42211700 frameshift variant -/C delins 0.700 0
dbSNP: rs1553511224
rs1553511224
10 0.882 0.080 2 161423825 frameshift variant -/C delins 0.700 0
dbSNP: rs372949028
rs372949028
13 0.827 0.240 22 20061684 splice donor variant G/A;C snv 7.1E-05 5.6E-05 0.700 1.000 1 2016 2016
dbSNP: rs1569301036
rs1569301036
17 0.827 0.240 X 71397354 missense variant C/T snv 0.700 0
dbSNP: rs1057518786
rs1057518786
5 1.000 6 33441374 splice region variant G/A snv 0.700 0
dbSNP: rs1057519444
rs1057519444
5 0.925 0.120 22 32518208 missense variant GG/AA mnv 0.700 0
dbSNP: rs782609482
rs782609482
4 1.000 0.120 9 133352060 splice donor variant C/A;T snv 4.1E-06 0.700 0
dbSNP: rs794727792
rs794727792
8 0.827 0.120 9 127661140 stop gained C/A;T snv 4.0E-06 0.700 0
dbSNP: rs796052243
rs796052243
54 0.695 0.520 4 122934574 inframe deletion CAA/- delins 0.700 0
dbSNP: rs1057518845
rs1057518845
5 0.925 0.120 12 23755726 splice acceptor variant T/G snv 0.700 0
dbSNP: rs1057518928
rs1057518928
3 1.000 0.040 12 23665471 missense variant G/A snv 0.700 0
dbSNP: rs1558373252
rs1558373252
19 0.790 0.120 2 5693013 frameshift variant T/- delins 0.700 0
dbSNP: rs1561498701
rs1561498701
5 1.000 0.080 5 70925150 frameshift variant -/GGATTCCG delins 0.700 1.000 1 2013 2013