{{Rsnum
|rsid=199473678
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CTC1
|position=8230304
|Gene_s=CTC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=17
|CLNALLE=1
|CLNDBN=Cerebroretinal microangiopathy with calcifications and cysts
|CLNDSDB=OMIM
|CLNDSDBID=612199
|CLNHGVS=NC_000017.10:g.8133622T>C
|CLNORIGIN=2
|CLNSIG=5
|Disease=Cerebroretinal microangiopathy with calcifications and cysts
|FwdALT=G
|FwdREF=A
|GENEINFO=CTC1:80169
|GENE_ID=80169
|GENE_NAME=CTC1
|REF=T
|RSPOS=8133622
|Reversed=1
|SAO=3
|SSR=0
|Tags=RV;PM;PMC;NSM;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000a01000002110120
|WGT=1
|dbSNPBuildID=136
|rsid=199473678
}}{{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
}}