{{Rsnum
|rsid=104894398
|Chromosome=13
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=GJB2
|position=20189443
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GJB2
}}{{omim
|id=121011
|rsnum=104894398
|variant=0006
}}{{ClinVar
|rsid=104894398
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=20763582
|CHROM=13
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=GJB2:2706
|GENE_NAME=GJB2
|GENE_ID=2706
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.20763582C>A
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=5096; 121011.0006
|CLNSIG=5
|CLNCUI=C2673759
|CLNDBN=Deafness, autosomal recessive 1A; Hereditary hearing loss and deafness; not provided
|Disease=Deafness; Hereditary hearing loss and deafness; not provided
|CLNACC=RCV000018529.27; RCV000037816.1; RCV000080366.1
|Tags=RV;PM;PMC;S3D;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=9336442
|Title=Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.
}}

{{PMID Auto
|PMID=10905664
|Title=Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates.
}}

{{PMID Auto
|PMID=11556849
|Title=Connexin 26 studies in patients with sensorineural hearing loss.
}}