{{Rsnum
|rsid=397517452
|Chromosome=10
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PCDH15
|position=54079426
|Gene_s=PCDH15
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=10
|CLNACC=RCV000039708.1
|CLNALLE=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
|CLNHGVS=NC_000010.10:g.55839186T>C
|CLNSIG=5
|Disease=Hereditary hearing loss and deafness; Retinitis pigmentosa-deafness syndrome
|FwdALT=G
|FwdREF=A
|GENEINFO=PCDH15:65217
|GENE_ID=65217
|GENE_NAME=PCDH15
|REF=T
|RSPOS=55839186
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=397517452
}}