WT1, WT1 transcription factor, 7490

N. diseases: 446; N. variants: 61
Disease: Frasier Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1049509674
rs1049509674
Entrez Id: 7490;51352
Gene Symbol: WT1;WT1-AS
WT1;WT1-AS
CUI: C0950122
Disease:
Frasier Syndrome 		0.010 GeneticVariation BEFREE analysis of the Wilms' tumour suppressor gene in a patient with Frasier syndrome by the polymerase chain reaction and direct sequencing detected a + 5G -->A transition at a position of the second alternative splice region of exon 9, important for predicting the risk of the occurrence of Wilms' tumour. 11954756 2002