{{Rsnum
|rsid=111033258
|Chromosome=3
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CLRN1
|position=150972565
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLRN1,CLRN1-AS1
}}{{omim
|id=606397
|rsnum=111033258
|variant=0004
}}{{ClinVar
|rsid=111033258
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=150690352
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=CLRN1:7401
|GENE_NAME=CLRN1
|GENE_ID=7401
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.150690352A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606397.0004
|CLNSIG=5
|CLNCUI=C1568248
|CLNDBN=Usher syndrome, type 3; Retinitis pigmentosa-deafness syndrome
|Disease=Usher syndrome; Retinitis pigmentosa-deafness syndrome
|CLNACC=RCV000004645.1; RCV000041432.1
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet; MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=C1568248:276902:231183:886; C0271097:500004:231183:886:57838006
}}{{PMID Auto
|PMID=12080385
|Title=USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses.
}}

{{PMID Auto
|PMID=12145752
|Title=Usher syndrome type III: revised genomic structure of the USH3 gene and identification of novel mutations.
|OA=1
}}

{{PMID Auto
|PMID=14569126
|Title=Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type III.
|OA=1
}}