{{Rsnum
|rsid=121908143
|Chromosome=3
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CLRN1
|position=150972591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLRN1,CLRN1-AS1
}}{{omim
|id=606397
|rsnum=121908143
|variant=0008
}}{{ClinVar
|rsid=121908143
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=150690378
|CHROM=3
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CLRN1:7401
|GENE_NAME=CLRN1
|GENE_ID=7401
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.150690378A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606397.0008
|CLNSIG=5
|CLNCUI=C1568248
|CLNDBN=Usher syndrome, type 3
|Disease=Usher syndrome
|CLNACC=RCV000004649.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1568248:276902:231183:886
}}