{{Rsnum
|rsid=137853001
|Chromosome=10
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PCDH15
|position=54664256
|Gene_s=PCDH15
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=605514
|variant=0002
|rsnum=137853001
}}{{ClinVar
|rsid=137853001
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=56424016
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PCDH15:65217
|GENE_NAME=PCDH15
|GENE_ID=65217
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.56424016G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605514.0002
|CLNSIG=5
|CLNCUI=C1865885
|CLNDBN=Usher syndrome, type 1F
|Disease=Usher syndrome
|CLNACC=RCV000005216.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1265:C1865885:602083:231169:886
}}