{{Rsnum
|rsid=80338943
|Chromosome=13
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=GJB2
|position=20189347
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GJB2
}}{{omim
|id=121011
|rsnum=80338943
|variant=0014
}}{{ClinVar
|rsid=80338943
|Reversed=1
|FwdREF=C
|FwdALT=
|REF=AG
|ALT=A
|RSPOS=20763485
|CHROM=13
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|GENEINFO=GJB2:2706
|GENE_NAME=GJB2
|GENE_ID=2706
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.20763486delG
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1272; 121011.0014
|CLNSIG=5
|CLNCUI=C2673759; C2673761; C1844678
|CLNDBN=Deafness, autosomal recessive 1A; Deafness, digenic, GJB2/GJB3; Hereditary hearing loss and deafness
|Disease=Deafness; Hereditary hearing loss and deafness
|CLNACC=RCV000018538.26; RCV000018539.22; RCV000037827.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; MedGen; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1272:NBK1434:C2673759:220290:90636; C2673761; NBK1434:C0236038:95827002
}}{{PMID|12384}} [Nursing and drugs: criticism of total dependence on analgesics for the treatment of pain. Reevaluation of nursing concession to the patient's request, resulting in the development of narcotic dependence].

{{PMID|10607953}} Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population.

{{PMID|10633133|OA=1
}} Prevalent connexin 26 gene (GJB2) mutations in Japanese.

{{PMID|16380907|OA=1
}} GJB2 mutations and degree of hearing loss: a multicenter study.

{{PMID|17505205}} The prevalence of the 235delC GJB2 mutation in a Chinese deaf population.

{{PMID|19050930|OA=1
}} Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31.