WT1, WT1 transcription factor, 7490

N. diseases: 446; N. variants: 61
Disease: WAGR Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121907909
rs121907909
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C0206115
Disease:
WAGR Syndrome 		A 0.700 CausalMutation CLINVAR Genetic screening in adolescents with steroid-resistant nephrotic syndrome. 23515051 2013
dbSNP: rs121907909
rs121907909
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C0206115
Disease:
WAGR Syndrome 		A 0.700 CausalMutation CLINVAR Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children. 21851196 2011
dbSNP: rs121907909
rs121907909
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C0206115
Disease:
WAGR Syndrome 		A 0.700 CausalMutation CLINVAR Exon 9 mutations in the WT1 gene, without influencing KTS splice isoforms, are also responsible for Frasier syndrome. 10571943 1999
dbSNP: rs121907909
rs121907909
Entrez Id: 7490
Gene Symbol: WT1
WT1
CUI: C0206115
Disease:
WAGR Syndrome 		A 0.700 CausalMutation CLINVAR Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology. 9108089 1997