{{Rsnum
|rsid=111033335
|Chromosome=13
|Orientation=minus
|geno1=(CAGTGTTCATGACATTC;CAGTGTTCATGACATTC)
|geno2=(CAGTGTTCATGACATTC;GTGTCTGGA)
|geno3=(GTGTCTGGA;GTGTCTGGA)
|Gene=GJB2
|position=20188982
|Gene_s=GJB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033335
|Reversed=1
|FwdREF=GTGTCTGGA
|FwdALT=CAGTGTTCATGACATTC
|REF=TTCCAGACAC
|ALT=TGAATGTCATGAACACTG
|RSPOS=20763120
|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.20763121_20763129delTCCAGACACinsGAATGTCATGAACACTG
|CLNORIGIN=1
|CLNSIG=4
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000037866.1
|CLNDBN=Hereditary hearing loss and deafness
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1434:C0236038:95827002
|Disease=Hereditary hearing loss and deafness
}}{{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
}}