{{Rsnum
|rsid=28931593
|Gene=GJB2
|Chromosome=13
|position=20189358
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GJB2
}}[[deafness]]
{{omim
|desc=KERATODERMA, PALMOPLANTAR, WITH DEAFNESS
|id=121011
|rsnum=28931593
|variant=0026
}}
{{ neighbor
| rsid = 28931592
| distance = 252
}}
{{ neighbor
| rsid = 28931594
| distance = 76
}}

{{ClinVar
|rsid=28931593
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=20763497
|CHROM=13
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GJB2:2706
|GENE_NAME=GJB2
|GENE_ID=2706
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.20763497C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=121011.0026
|CLNSIG=5
|CLNCUI=C1835672; C2675750
|CLNDBN=Keratoderma palmoplantar deafness; Deafness, autosomal dominant 3a
|Disease=Keratoderma palmoplantar deafness; Deafness
|CLNACC=RCV000018554.26; RCV000018555.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C1835672:148350:2202; NBK1434:NBK1536:C2675750:601544:90635
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}