rs1037084691, WT1

N. diseases: 5
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.
NEPHROTIC SYNDROME, TYPE 4
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
9 0.827 0.160 11 32392031 missense variant C/G;T snv 0.700 0
Hypospadias
CUI: C0848558
Disease: Hypospadias
80 0.827 0.160 11 32392031 missense variant C/G;T snv 0.010 1.000 1 2019 2019
Hypospadias, perineal
CUI: C0452148
Disease: Hypospadias, perineal
15 0.827 0.160 11 32392031 missense variant C/G;T snv 0.010 1.000 1 2019 2019
Nephroblastoma
CUI: C0027708
Disease: Nephroblastoma
125 0.827 0.160 11 32392031 missense variant C/G;T snv 0.010 1.000 1 2015 2015
Penile hypospadias
CUI: C1691215
Disease: Penile hypospadias
83 0.827 0.160 11 32392031 missense variant C/G;T snv 0.010 1.000 1 2019 2019