{{Rsnum
|rsid=139675596
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=C5orf42
|position=37165595
|Gene_s=C5orf42
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=5
|CLNACC=RCV000024222.2
|CLNALLE=1
|CLNDBN=Joubert syndrome 17
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1325:CN124733:614615:475
|CLNHGVS=NC_000005.9:g.37165697G>A
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1325; 614571.0005
|Disease=Joubert syndrome 17
|FwdALT=A
|FwdREF=G
|GENEINFO=C5orf42:65250
|GENE_ID=65250
|GENE_NAME=C5orf42
|REF=G
|RSPOS=37165697
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=139675596
}}{{PMID Auto
|PMID=22425360
|Title=Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population.
|OA=1
}}