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: rs121907908
rs121907908
WT1
1 1.000 0.040 11 32400025 missense variant T/A;C snv 0.700 0
dbSNP: rs387906350
rs387906350
3 0.882 0.120 1 85267830 frameshift variant A/-;AA delins 0.700 0
dbSNP: rs387906351
rs387906351
3 0.882 0.160 1 85270828 frameshift variant T/-;TT delins 0.700 0
dbSNP: rs104894094
rs104894094
12 0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 0.010 1.000 1 2016 2016