{{Rsnum
|rsid=118204052
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CC2D2A
|position=15599614
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CC2D2A
}}{{omim
|id=612013
|rsnum=118204052
|variant=0004
}}{{ClinVar
|rsid=118204052
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=15601237
|CHROM=4
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CC2D2A:57545
|GENE_NAME=CC2D2A
|GENE_ID=57545
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.15601237C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612013.0004
|CLNSIG=5
|CLNCUI=C2676788
|CLNDBN=Joubert syndrome 9
|Disease=Joubert syndrome 9
|CLNACC=RCV000000780.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2676788:612285:2318
}}