{{Rsnum
|rsid=121908140
|Gene=CLRN1
|Chromosome=3
|position=150928107
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=CLRN1
}}{{omim
|id=606397
|rsnum=121908140
|variant=0001
}}{{ClinVar
|rsid=121908140
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=150645894
|CHROM=3
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=CLRN1:7401
|GENE_NAME=CLRN1
|GENE_ID=7401
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.150645894A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606397.0001
|CLNSIG=5
|CLNCUI=C1568248
|CLNDBN=Usher syndrome, type 3
|Disease=Usher syndrome
|CLNACC=RCV000004642.1
|Tags=RV;PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1568248:276902:231183:886
|COMMON=0
}}