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: 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: rs121907910
rs121907910
WT1
1 1.000 0.160 11 32392705 missense variant G/A snv 0.700 0