rs267602852, WT1

N. diseases: 7
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.
Ambiguous Genitalia
CUI: C0266362
Disease: Ambiguous Genitalia
14 0.827 0.160 11 32417631 missense variant G/A snv 0.700 0
Focal glomerulosclerosis
CUI: C0017668
Disease: Focal glomerulosclerosis
50 0.827 0.160 11 32417631 missense variant G/A snv 0.700 0
Frasier Syndrome
CUI: C0950122
Disease: Frasier Syndrome
17 0.827 0.160 11 32417631 missense variant G/A snv 0.700 0
Glomerulonephritis
CUI: C0017658
Disease: Glomerulonephritis
7 0.827 0.160 11 32417631 missense variant G/A snv 0.700 0
Nephrosis, congenital
CUI: C3501848
Disease: Nephrosis, congenital
9 0.827 0.160 11 32417631 missense variant G/A snv 0.700 0
Proteinuria
CUI: C0033687
Disease: Proteinuria
20 0.827 0.160 11 32417631 missense variant G/A snv 0.700 0
Serum creatinine raised
CUI: C0700225
Disease: Serum creatinine raised
2 0.827 0.160 11 32417631 missense variant G/A snv 0.700 0