{{Rsnum
|rsid=2728726
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=DKC1
|position=154770804
|Gene_s=DKC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 1.0 | 99.0
| HapMapRevision=28
}}{{ClinVar
|ALT=A,G
|CHROM=X
|CLNACC=RCV000032209.2
|CLNALLE=2
|CLNDBN=Dyskeratosis congenita X-linked
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK22301:C1148551:305000
|CLNHGVS=NC_000023.10:g.153999079C>G
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=GeneReviews; UniProtKB (variants)
|CLNSRCID=NBK22301; VAR_010081
|Disease=Dyskeratosis congenita X-linked
|FwdALT=A,G
|FwdREF=C
|GENEINFO=DKC1:1736
|GENE_ID=1736
|GENE_NAME=DKC1
|REF=C
|RSPOS=153999079
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;VLD;HD;GNO;OTHERKG;PH3;LSD;OM
|VC=SNV
|VP=0x050368000000040503110100
|WGT=0
|dbSNPBuildID=100
|rsid=2728726
}}

{{PMID Auto
|PMID=10364516
|Title=X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene.
|OA=1
}}

{{on chip | Illumina Human 1M}}