{{Rsnum
|rsid=199469706
|Chromosome=10
|Orientation=minus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=PCDH15
|position=54213948
|Gene_s=PCDH15
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199469706
|Reversed=1
|FwdREF=T
|FwdALT=
|REF=CA
|ALT=C
|RSPOS=55973705
|CHROM=10
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002110200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.55973708delA
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605514.0003
|CLNSIG=5
|CLNCUI=C1865885
|CLNDBN=Usher syndrome, type 1F
|Disease=Usher syndrome
|CLNACC=RCV000005217.1
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1265:C1865885:602083:231169:886
|GENEINFO=PCDH15:65217
|GENE_ID=65217
|GENE_NAME=PCDH15
}}{{PMID Auto
|PMID=11487575
|Title=Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.
}}