{{Rsnum
|rsid=111294855
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=C5orf42
|position=37157382
|Gene_s=C5orf42
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=5
|CLNACC=RCV000024223.1; RCV000034938.1
|CLNALLE=1
|CLNDBN=Variant of unknown significance; Joubert syndrome 17
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1325:CN124733:614615:475
|CLNHGVS=NC_000005.9:g.37157484C>T
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1325; 614571.0006
|Disease=Variant of unknown significance; Joubert syndrome 17
|FwdALT=T
|FwdREF=C
|GENEINFO=C5orf42:65250
|GENE_ID=65250
|GENE_NAME=C5orf42
|REF=C
|RSPOS=37157484
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;VLD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000040002110100
|WGT=0
|dbSNPBuildID=132
|rsid=111294855
}}{{PMID Auto
|PMID=22425360
|Title=Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population.
|OA=1
}}