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: rs386833945
rs386833945
4 0.882 0.080 19 35850987 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
dbSNP: rs71785313
rs71785313
5 0.882 0.120 22 36265996 inframe deletion TTATAA/- delins 0.700 0
dbSNP: rs759191907
rs759191907
25 0.776 0.360 9 127825225 splice region variant A/G snv 8.0E-06 0.700 0
dbSNP: rs749740335
rs749740335
3 0.925 0.080 1 179552620 frameshift variant TT/- delins 6.8E-05 9.1E-05 0.700 0
dbSNP: rs74315342
rs74315342
10 0.763 0.120 1 179561327 missense variant C/T snv 6.0E-04 5.3E-04 0.700 0