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 High-resolution temporal bone CT scans of children (n = 21) with DFNB1 SNHL were compared to age-matched controls with either conductive hearing loss (CHL, n = 33) or a nonsyndromic, non-DFNB1 SNHL (n = 33). 25583854 2015
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.120 GeneticVariation disease LHGDN This points to the possibility that the Cx26 D50N mutation can cause conductive hearing loss. 18412859 2008
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.120 GeneticVariation disease BEFREE This points to the possibility that the Cx26 D50N mutation can cause conductive hearing loss. 18412859 2008
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.120 Biomarker disease HPO