{{Rsnum
|rsid=199473673
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CTC1
|position=8237487
|Gene_s=CTC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=17
|CLNACC=RCV000023995.2
|CLNALLE=1
|CLNDBN=Cerebroretinal microangiopathy with calcifications and cysts
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2677299:612199:313838
|CLNHGVS=NC_000017.10:g.8140805G>A
|CLNORIGIN=2
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613129.0010
|Disease=Cerebroretinal microangiopathy with calcifications and cysts
|FwdALT=T
|FwdREF=C
|GENEINFO=CTC1:80169
|GENE_ID=80169
|GENE_NAME=CTC1
|REF=G
|RSPOS=8140805
|Reversed=1
|SAO=3
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110120
|WGT=0
|dbSNPBuildID=136
|rsid=199473673
}}{{PMID Auto
|PMID=22387016
|Title=Mutations in CTC1, encoding the CTS telomere maintenance complex component 1, cause cerebroretinal microangiopathy with calcifications and cysts.
|OA=1
}}