{{Rsnum
|rsid=121912608
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ARL13B
|position=94036663
|Gene_s=ARL13B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=608922
|rsnum=121912608
|variant=0003
}}{{ClinVar
|rsid=121912608
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=93755507
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ARL13B:200894
|GENE_NAME=ARL13B
|GENE_ID=200894
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.93755507C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608922.0003
|CLNSIG=5
|CLNCUI=C2676771
|CLNDBN=Joubert syndrome 8
|Disease=Joubert syndrome 8
|CLNACC=RCV000002070.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1325:C2676771:612291:475
}}