Source: ALL
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: rs587776576
rs587776576
WT1
7 0.790 0.280 11 32391967 splice region variant C/T snv 0.700 1.000 1 1992 1992
dbSNP: rs1037084691
rs1037084691
WT1
5 0.827 0.160 11 32392031 missense variant C/G;T snv 0.700 0
dbSNP: rs121907900
rs121907900
WT1
11 0.763 0.200 11 32392020 missense variant G/A snv 0.700 0
dbSNP: rs121907906
rs121907906
WT1
8 0.776 0.320 11 32392717 stop gained G/A snv 0.700 0
dbSNP: rs1554939785
rs1554939785
WT1
1 1.000 11 32396262 missense variant T/G snv 0.700 0
dbSNP: rs28941777
rs28941777
WT1
2 0.925 0.160 11 32392053 missense variant A/G snv 0.700 0
dbSNP: rs28941778
rs28941778
WT1
2 0.925 0.200 11 32392014 missense variant C/A;T snv 0.700 0
dbSNP: rs28942089
rs28942089
WT1
2 0.925 0.200 11 32392672 missense variant G/A snv 0.700 0
dbSNP: rs587776577
rs587776577
WT1
3 0.925 0.160 11 32391968 splice region variant G/A snv 0.700 0