Gene: SMARCB1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6598
Gene Symbol: SMARCB1
SMARCB1 		0.110 GeneticVariation group BEFREE The mutations were associated with syndromic ID and speech impairment (severe/profound in SMARCB1, SMARCE1, and ARID1A mutations; variable in SMARCA4, SMARCA2, and ARID1B mutations), which was frequently accompanied by agenesis or hypoplasia of the corpus callosum. 23637025 2013
Entrez Id: 6598
Gene Symbol: SMARCB1
SMARCB1 		0.110 Biomarker group HPO