Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.700 Biomarker disease GENOMICS_ENGLAND ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249 2013
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.700 GermlineCausalMutation disease ORPHANET WT1 in disease: shifting the epithelial-mesenchymal balance. 21959952 2012
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.700 GermlineCausalMutation disease ORPHANET WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations. 17853480 2007
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.700 GeneticVariation disease UNIPROT WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations. 17853480 2007
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.700 Biomarker disease CTD_human
Entrez Id: 7490
Gene Symbol: WT1
WT1 		0.700 CausalMutation disease CLINVAR