Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121907900
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv
CUI: C0950121
Disease: Denys-Drash Syndrome
Denys-Drash Syndrome 		0.710 1.000 1 2017 2017
dbSNP: rs121907900
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv
CUI: C0445118
Disease: Nephrotic range proteinuria
Nephrotic range proteinuria 		0.700 0
dbSNP: rs121907900
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv
CUI: C0403397
Disease: Steroid-resistant nephrotic syndrome
Steroid-resistant nephrotic syndrome 		0.700 0
dbSNP: rs121907900
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder) 		0.700 0
dbSNP: rs121907900
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv
CUI: C0950122
Disease: Frasier Syndrome
Frasier Syndrome 		0.700 0
dbSNP: rs121907900
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		0.700 0
dbSNP: rs121907900
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		0.700 0
dbSNP: rs121907900
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
46, XY Disorders of Sex Development 		0.010 1.000 1 2017 2017
dbSNP: rs121907900
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv
CUI: C1691215
Disease: Penile hypospadias
Penile hypospadias 		0.010 1.000 1 2017 2017
dbSNP: rs121907900
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv
CUI: C0848558
Disease: Hypospadias
Hypospadias 		0.010 1.000 1 2017 2017
dbSNP: rs121907900
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv
CUI: C0206661
Disease: Gonadoblastoma
Gonadoblastoma 		0.010 1.000 1 2017 2017