Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3913
Gene Symbol: LAMB2
LAMB2 		0.700 Biomarker disease GENOMICS_ENGLAND Genetic investigation of 93 families with microphthalmia or posterior microphthalmos. 29450879 2018
Entrez Id: 3913
Gene Symbol: LAMB2
LAMB2 		0.700 GeneticVariation disease UNIPROT A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome. 21236492 2011
Entrez Id: 3913
Gene Symbol: LAMB2
LAMB2 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum. 20556798 2010
Entrez Id: 3913
Gene Symbol: LAMB2
LAMB2 		0.700 GeneticVariation disease UNIPROT Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome. 20798252 2010
Entrez Id: 3913
Gene Symbol: LAMB2
LAMB2 		0.700 GeneticVariation disease CLINVAR Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum. 20556798 2010
Entrez Id: 3913
Gene Symbol: LAMB2
LAMB2 		0.700 CausalMutation disease CLINVAR
Entrez Id: 3913
Gene Symbol: LAMB2
LAMB2 		0.700 Biomarker disease CTD_human