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: rs121907900
rs121907900
WT1
4 0.846 0.214 11 32392020 missense variant G/A snp 0.700 9 1983 2017
dbSNP: rs121907909
rs121907909
WT1
3 0.878 0.250 11 32392032 stop gained G/A snp 0.700 5 1997 2017
dbSNP: rs28941778
rs28941778
WT1
2 0.923 0.214 11 32392014 missense variant C/T snp 0.700 4 1991 1998
dbSNP: rs121907901
rs121907901
WT1
1 1.000 0.179 11 32392704 missense variant C/T snp 0.700 3 1991 2008
dbSNP: rs121907906
rs121907906
WT1
1 1.000 0.179 11 32392717 stop gained G/A snp 0.700 2 1996 1997
dbSNP: rs28942089
rs28942089
WT1
2 0.923 0.214 11 32392672 missense variant G/A snp 0.700 2 1992 1998
dbSNP: rs1060501253
rs1060501253
WT1
2 0.923 0.179 11 32428031 frameshift variant CG/C in-del 0.700 1 2017 2017
dbSNP: rs121907902
rs121907902
WT1
1 1.000 0.179 11 32392013 missense variant T/C snp 0.700 1 1991 1991
dbSNP: rs121907903
rs121907903
WT1
1 1.000 0.179 11 32392019 missense variant C/G,T snp 0.700 1 1993 1993
dbSNP: rs121907904
rs121907904
WT1
1 1.000 0.179 11 32396313 missense variant C/T snp 0.700 1 1993 1993
dbSNP: rs121907905
rs121907905
WT1
1 1.000 0.179 11 32392723 missense variant A/C snp 0.700 1 1997 1997
dbSNP: rs121907907
rs121907907
WT1
1 1.000 0.179 11 32392682 missense variant G/A,C snp 4.0E-06 0.700 1 1997 1997
dbSNP: rs587776576
rs587776576
WT1
4 0.846 0.214 11 32391967 splice region variant C/T snp 0.700 1 1993 1993
dbSNP: rs760336723
rs760336723
3 0.878 0.214 7 131506292 missense variant G/A snp 2.8E-05 3.2E-05 0.010 1.000 1 2004 2004