{{Rsnum
|rsid=121912302
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=DKC1
|position=154765480
|Gene_s=DKC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000032191.2
|CLNALLE=1
|CLNDBN=Dyskeratosis congenita X-linked
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK22301:C1148551:305000
|CLNHGVS=NC_000023.10:g.153993755G>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=GeneReviews; UniProtKB (variants)
|CLNSRCID=NBK22301; VAR_010078
|Disease=Dyskeratosis congenita X-linked
|FwdALT=A
|FwdREF=G
|GENEINFO=DKC1:1736
|GENE_ID=1736
|GENE_NAME=DKC1
|REF=G
|RSPOS=153993755
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=121912302
}}{{PMID Auto
|PMID=10364516
|Title=X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene.
|OA=1
}}