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: rs387907144
rs387907144
34 0.716 0.600 6 157181056 stop gained C/A;T snv 0.700 1.000 2 2012 2015
dbSNP: rs1135401778
rs1135401778
20 0.752 0.400 17 67854315 frameshift variant T/- del 0.700 1.000 1 2017 2017
dbSNP: rs1057518879
rs1057518879
19 0.776 0.280 1 11965571 stop gained G/A snv 0.700 0
dbSNP: rs1057518918
rs1057518918
6 0.882 0.160 6 157184329 frameshift variant C/- delins 0.700 0
dbSNP: rs387906271
rs387906271
11 0.790 0.320 8 60801598 splice region variant G/C snv 0.700 0
dbSNP: rs763028380
rs763028380
12 0.851 0.320 11 17453271 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 0.700 0
dbSNP: rs6523
rs6523
4 0.882 0.200 19 17821329 missense variant T/C snv 0.65 0.70 0.020 < 0.001 2 2007 2016
dbSNP: rs1423753702
rs1423753702
WT1
6 0.807 0.280 11 32396401 stop gained G/A snv 1.4E-05 0.010 1.000 1 2009 2009
dbSNP: rs144670595
rs144670595
2 0.925 0.120 19 920441 missense variant G/T snv 3.3E-04 4.5E-04 0.010 1.000 1 2018 2018