{{Rsnum
|rsid=121908353
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CDH23
|position=71812822
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CDH23
}}{{omim
|id=605516
|rsnum=121908353
|variant=0012
}}{{ClinVar
|rsid=121908353
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=73572579
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CDH23:64072
|GENE_NAME=CDH23
|GENE_ID=64072
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.73572579C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000005209.1; RCV000039312.1
|CLNDBN=USHER SYNDROME, TYPE ID/F, DIGENIC; AllHighlyPenetrant
|CLNDSDB=MedGen
|CLNDSDBID=CN169374
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605516.0012
|Disease=USHER SYNDROME; AllHighlyPenetrant
}}