{{Rsnum
|rsid=281865158
|Chromosome=8
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=WRN
|position=31111705
|Gene_s=WRN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CT
|CHROM=8
|CLNACC=RCV000032136.1
|CLNALLE=1
|CLNDBN=Werner syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1514:C0043119:277700:902:51626007
|CLNHGVS=NC_000008.10:g.30969221dupT
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1514
|Disease=Werner syndrome
|FwdALT=T
|REF=C
|RSPOS=30969220
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=281865158
|GENEINFO=WRN:7486
|GENE_ID=7486
|GENE_NAME=WRN
}}{{PMID Auto
|PMID=16673358
|Title=The spectrum of WRN mutations in Werner syndrome patients.
|OA=1
}}

{{PMID Auto
|PMID=20443122
|Title=WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.
}}