{{Rsnum
|rsid=80338942
|Chromosome=13
|Orientation=minus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=GJB2
|position=20189415
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GJB2
}}{{omim
|id=121011
|rsnum=80338942
|variant=0010
}}{{ClinVar
|rsid=80338942
|Reversed=1
|FwdREF=T
|FwdALT=
|REF=CA
|ALT=C
|RSPOS=20763553
|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.20763554delA
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1272; 121011.0010
|CLNSIG=5
|CLNCUI=C1844678
|CLNDBN=Deafness, autosomal recessive 1A; Hereditary hearing loss and deafness
|Disease=Deafness; Hereditary hearing loss and deafness
|CLNACC=RCV000018534.27; RCV000037817.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1272:NBK1434:C2673759:220290:90636; NBK1434:C0236038:95827002
}}{{PMID Auto
|PMID=9819448
|Title=Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness.
}}

{{PMID Auto
|PMID=10903123
|Title=Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT.
|OA=1
}}

{{PMID Auto
|PMID=110744
|Title=Hydroxyurea or placebo combined with radiation to treat stages IIIB and IV cervical cancer confined to the pelvis.
}}

{{PMID Auto
|PMID=10508996
|Title=High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim.
}}

{{PMID Auto
|PMID=10982182
|Title=The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population.
}}

{{PMID Auto
|PMID=11386851
|Title=Nonradioactive detection of the common Connexin 26 167delT and 35delG mutations and frequencies among Ashkenazi Jews.
}}

{{PMID Auto
|PMID=11668644
|Title=A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews.
}}