rs121907900, WT1

N. diseases: 11
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Denys-Drash Syndrome
CUI: C0950121
Disease: Denys-Drash Syndrome
24 0.763 0.200 11 32392020 missense variant G/A snv 0.710 1.000 1 2017 2017
Frasier Syndrome
CUI: C0950122
Disease: Frasier Syndrome
17 0.763 0.200 11 32392020 missense variant G/A snv 0.700 0
MEACHAM SYNDROME (disorder)
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
3 0.763 0.200 11 32392020 missense variant G/A snv 0.700 0
Nephroblastoma
CUI: C0027708
Disease: Nephroblastoma
125 0.763 0.200 11 32392020 missense variant G/A snv 0.700 0
Nephrotic range proteinuria
CUI: C0445118
Disease: Nephrotic range proteinuria
7 0.763 0.200 11 32392020 missense variant G/A snv 0.700 0
NEPHROTIC SYNDROME, TYPE 4
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
9 0.763 0.200 11 32392020 missense variant G/A snv 0.700 0
Steroid-resistant nephrotic syndrome
25 0.763 0.200 11 32392020 missense variant G/A snv 0.700 0
46, XY Disorders of Sex Development
CUI: C2751824
Disease: 46, XY Disorders of Sex Development
10 0.763 0.200 11 32392020 missense variant G/A snv 0.010 1.000 1 2017 2017
Gonadoblastoma
CUI: C0206661
Disease: Gonadoblastoma
2 0.763 0.200 11 32392020 missense variant G/A snv 0.010 1.000 1 2017 2017
Hypospadias
CUI: C0848558
Disease: Hypospadias
80 0.763 0.200 11 32392020 missense variant G/A snv 0.010 1.000 1 2017 2017
Penile hypospadias
CUI: C1691215
Disease: Penile hypospadias
83 0.763 0.200 11 32392020 missense variant G/A snv 0.010 1.000 1 2017 2017