rs1188182005, WT1

N. diseases: 2
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.
Frasier Syndrome
CUI: C0950122
Disease: Frasier Syndrome
17 0.925 0.200 11 32430535 missense variant T/C snv 4.2E-06 7.1E-06 0.010 1.000 1 2002 2002
Nephroblastoma
CUI: C0027708
Disease: Nephroblastoma
125 0.925 0.200 11 32430535 missense variant T/C snv 4.2E-06 7.1E-06 0.010 1.000 1 2002 2002