{{Rsnum
|rsid=386834156
|Chromosome=12
|position=88136702
|Orientation=minus
|geno1=(AG;AG)
|geno2=(AG;T)
|geno3=(T;T)
|Gene=CEP290
|Gene_s=CEP290
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=TA
|CHROM=12
|CLNACC=RCV000050150.1
|CLNALLE=1
|CLNDBN=Meckel syndrome type 4
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1970161:611134:564
|CLNHGVS=NC_000012.11:g.88530479_88530480delCTinsA
|CLNSIG=4
|Disease=Meckel syndrome type 4
|FwdALT=T
|FwdREF=AG
|REF=TCT
|RSPOS=88530478
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386834156
|GENEINFO=CEP290:80184
|GENE_ID=80184
|GENE_NAME=CEP290
}}{{PMID Auto
|PMID=17564974
|Title=Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndrome.
|OA=1
}}