{{Rsnum
|rsid=386833764
|Gene=CC2D2A
|Chromosome=4
|position=15511391
|Orientation=plus
|GMAF=0.04178
|Gene_s=CC2D2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(-;-)
|geno2=(-;GAA)
|geno3=(GAA;GAA)
}}{{ClinVar
|ALT=G
|CAF=0.9582; 0.04178
|CHROM=4
|CLNACC=RCV000049728.1; RCV000079448.1
|CLNALLE=1
|CLNDBN=Meckel syndrome, type 6; AllHighlyPenetrant
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=C2676790:612284:564; CN169374
|CLNHGVS=NC_000004.11:g.15513014_15513016delGAA
|CLNSIG=4
|COMMON=1
|Disease=Meckel syndrome; AllHighlyPenetrant
|FwdREF=GAA
|REF=GGAA
|RSPOS=15513004
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833764
|GENEINFO=CC2D2A:57545
|GENE_ID=57545
|GENE_NAME=CC2D2A
}}{{PMID Auto
|PMID=21068128
|Title=Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy.
|OA=1
}}