{{Rsnum
|rsid=121912606
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ARL13B
|position=94003764
|Gene_s=ARL13B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=608922
|rsnum=121912606
|variant=0001
}}{{ClinVar
|rsid=121912606
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=93722608
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ARL13B:200894
|GENE_NAME=ARL13B
|GENE_ID=200894
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.93722608G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608922.0001
|CLNSIG=5
|CLNCUI=C2676771
|CLNDBN=Joubert syndrome 8
|Disease=Joubert syndrome 8
|CLNACC=RCV000002068.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1325:C2676771:612291:475
}}