{{Rsnum
|rsid=111033295
|Chromosome=13
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=GJB2
|position=20189217
|Gene_s=GJB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033295
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=20763356
|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.20763356T>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000037844.1; RCV000080375.1
|CLNDBN=Hereditary hearing loss and deafness; not provided
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1434:C0236038:95827002
|Disease=Hereditary hearing loss and deafness; not provided
|CLNSRC=Emory University
|CLNSRCID=302
}}{{PMID Auto
|PMID=10376574
|Title=Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.
}}

{{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=17041943
|Title=DNA sequence analysis of GJB2, encoding connexin 26: observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls.
|OA=1
}}

{{PMID Auto
|PMID=18776652
|Title=GJB2 mutations in Baluchi population.
}}