{{Rsnum
|rsid=111033267
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CLRN1
|position=150972520
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLRN1,CLRN1-AS1
}}{{omim
|id=606397
|rsnum=111033267
|variant=0006
}}{{ClinVar
|rsid=111033267
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=150690307
|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.150690307G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606397.0006
|CLNSIG=5
|CLNCUI=C1568248
|CLNDBN=Usher syndrome, type 3; Retinitis pigmentosa-deafness syndrome
|Disease=Usher syndrome; Retinitis pigmentosa-deafness syndrome
|CLNACC=RCV000004647.1; RCV000041433.1
|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=15521980
|Title=Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability.
}}