{{Rsnum
|rsid=111033299
|Chromosome=13
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GJB2
|position=20189299
|Gene_s=GJB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033299
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=20763438
|CHROM=13
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|GENEINFO=GJB2:2706
|GENE_NAME=GJB2
|GENE_ID=2706
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.20763438C>T
|CLNORIGIN=1
|CLNSIG=4
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000037834.1
|CLNDBN=Hereditary hearing loss and deafness
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1434:C0236038:95827002
|Disease=Hereditary hearing loss and deafness
}}{{PMID Auto
|PMID=169315
|Title=[A case of bronchial carcinoid with carcinoid syndrome (author transl)].
}}

{{PMID Auto
|PMID=9529365
|Title=Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.
|OA=1
}}

{{PMID Auto
|PMID=12865758
|Title=Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.
}}

{{PMID Auto
|PMID=14985372
|Title=A genotype-phenotype correlation for GJB2 (connexin 26) deafness.
|OA=1
}}

{{PMID Auto
|PMID=15967879
|Title=GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients.
}}

{{PMID Auto
|PMID=16222667
|Title=Connexin 26 variants and auditory neuropathy/dys-synchrony among children in schools for the deaf.
}}