{{Rsnum
|rsid=111033204
|Chromosome=13
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AT)
|geno3=(AT;AT)
|Gene=GJB2
|position=20189282
|Gene_s=GJB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033204
|Reversed=1
|FwdREF=AT
|FwdALT=
|REF=CAT
|ALT=C
|RSPOS=20763420
|CHROM=13
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002100200
|GENEINFO=GJB2:2706
|GENE_NAME=GJB2
|GENE_ID=2706
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.20763421_20763422delAT
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000037835.1
|CLNDBN=Hereditary hearing loss and deafness
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1434:C0236038:95827002
|Disease=Hereditary hearing loss and deafness
}}{{PMID|10633133|OA=1
}} Prevalent connexin 26 gene (GJB2) mutations in Japanese.

{{PMID|10983956}} Connexin26 mutations associated with nonsyndromic hearing loss.

{{PMID|11385713}} Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population.

{{PMID|11438992}} Assessment of denaturing high-performance liquid chromatography (DHPLC) in screening for mutations in connexin 26 (GJB2).

{{PMID|12111646}} Mutations of Cx26 gene (GJB2) for prelingual deafness in Taiwan.