{{Rsnum
|rsid=111033247
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CDH23
|position=71790414
|Gene_s=CDH23
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033247
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=73550171
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|GENEINFO=CDH23:64072
|GENE_NAME=CDH23
|GENE_ID=64072
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.73550171G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000039234.1
|CLNDBN=Hereditary hearing loss and deafness; Retinitis pigmentosa-deafness syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1434:C0236038:95827002; C0271097:500004:231183:886:57838006
|Disease=Hereditary hearing loss and deafness; Retinitis pigmentosa-deafness syndrome
}}{{PMID Auto
|PMID=11090341
|Title=Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
|OA=1
}}