{{Rsnum
|rsid=200879436
|Gene=CEP152
|Chromosome=15
|position=48768237
|Orientation=plus
|GMAF=0.002755
|Gene_s=CEP152
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|ALT=C
|CAF=0.9972; 0.002755
|CHROM=15
|CLNACC=RCV000024028.1
|CLNALLE=1
|CLNDBN=Seckel syndrome 5
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3151187:613823:808
|CLNHGVS=NC_000015.9:g.49060434T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613529.0007
|COMMON=1
|Disease=Seckel syndrome 5
|FwdALT=C
|FwdREF=T
|GENEINFO=CEP152:22995
|GENE_ID=22995
|GENE_NAME=CEP152
|REF=T
|RSPOS=49060434
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000416110100
|WGT=0
|dbSNPBuildID=137
|rsid=200879436
}}