Gene: GJB2 ×
Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.500 CausalMutation phenotype CLINVAR Homozygous M34T mutation of the GJB2 gene associates with an autosomal recessive nonsyndromic sensorineural hearing impairment in Finnish families. 22668073 2012
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.500 CausalMutation phenotype CLINVAR GJB2 mutations and degree of hearing loss: a multicenter study. 16380907 2005
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.500 GeneticVariation phenotype CLINVAR