{{Rsnum
|rsid=121912303
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=DKC1
|position=154762970
|Gene_s=DKC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=X
|CLNACC=RCV000032202.2
|CLNALLE=1
|CLNDBN=Dyskeratosis congenita X-linked
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK22301:C1148551:305000
|CLNHGVS=NC_000023.10:g.153991245C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=GeneReviews; UniProtKB (variants)
|CLNSRCID=NBK22301; VAR_010076
|Disease=Dyskeratosis congenita X-linked
|FwdALT=T
|FwdREF=C
|GENEINFO=DKC1:1736
|GENE_ID=1736
|GENE_NAME=DKC1
|REF=C
|RSPOS=153991245
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=121912303
}}{{PMID Auto
|PMID=10364516
|Title=X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene.
|OA=1
}}