Gene: GJB2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.120 GeneticVariation disease BEFREE The novel c.247_249delTTC (p.F83del) GJB2 mutation in a family with prelingual sensorineural deafness. 22484064 2012
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.120 GeneticVariation disease BEFREE Mutations in the GJB2 gene are the most common cause of hereditary prelingual sensorineural hearing impairment in Europe. 17671735 2007
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.120 GeneticVariation disease CLINVAR