{{Rsnum
|rsid=386833753
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CC2D2A
|position=15569290
|Gene_s=CC2D2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=4
|CLNACC=RCV000049717.1
|CLNALLE=1
|CLNDBN=Meckel syndrome, type 6
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2676790:612284:564
|CLNHGVS=NC_000004.11:g.15570913C>A
|CLNSIG=4
|Disease=Meckel syndrome
|FwdALT=A
|FwdREF=C
|REF=C
|RSPOS=15570913
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833753
|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
}}