{{Rsnum
|rsid=121908350
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CDH23
|position=71732151
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CDH23,C10orf105
}}{{omim
|id=605516
|rsnum=121908350
|variant=0007
}}{{ClinVar
|rsid=121908350
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=73491908
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=C10orf105:414152; CDH23:64072
|GENE_NAME=C10orf105; CDH23
|GENE_ID=414152; 64072
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.73491908C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605516.0007
|CLNSIG=5
|CLNCUI=C1832845
|CLNDBN=Usher syndrome, type 1D
|Disease=Usher syndrome
|CLNACC=RCV000005203.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1265:C1832845:601067:231169:886
}}