Gene: SMARCC2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6601
Gene Symbol: SMARCC2
SMARCC2 		0.410 GeneticVariation disease BEFREE Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay. 30580808 2019
Entrez Id: 6601
Gene Symbol: SMARCC2
SMARCC2 		0.410 Biomarker disease GENOMICS_ENGLAND Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay. 30580808 2019
Entrez Id: 6601
Gene Symbol: SMARCC2
SMARCC2 		0.410 Biomarker disease HPO