{{Rsnum
|rsid=386833750
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CC2D2A
|position=15563485
|Gene_s=CC2D2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G,T
|CHROM=4
|CLNACC=RCV000049714.1; RCV000000783.1; RCV000023922.1
|CLNALLE=1; 2
|CLNDBN=Meckel syndrome, type 6; COACH syndrome; Joubert syndrome 9/15, digenic
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=C2676790:612284:564; C1857662:216360:1454; CN121474
|CLNHGVS=NC_000004.11:g.15565108C>G; NC_000004.11:g.15565108C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=612013.0007
|Disease=Meckel syndrome; COACH syndrome; Joubert syndrome 9/15
|FwdALT=G,T
|FwdREF=C
|REF=C
|RSPOS=15565108
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833750
|GENEINFO=CC2D2A:57545
|GENE_ID=57545
|GENE_NAME=CC2D2A
}}{{PMID Auto
|PMID=19777577
|Title=CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation.
|OA=1
}}