{{Rsnum
|rsid=17847577
|Summary=Werner's Syndrome
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=8
|position=31081132
|Orientation=plus
|Gene=WRN
|Gene_s=WRN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}
[[rs17847577]], also known as R368X, Arg368Ter, Arg369Ter, c.1105C>T or 1336C>T) represents the most common [[WRN]] mutation seen in Caucasians as well as all other non-Japanese populations, perhaps representing ~20% of all Werner Syndrome cases.


{{omim
|id=604611
|rsnum=17847577
|variant=0006
}}

{{ClinVar
|rsid=17847577
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=30938648
|CHROM=8
|dbSNPBuildID=123
|SSR=0
|SAO=1
|VP=0x050168000000040102110100
|GENEINFO=WRN:7486
|GENE_NAME=WRN
|GENE_ID=7486
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.30938648C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1514; 604611.0006
|CLNSIG=5
|CLNCUI=C0043119
|CLNDBN=Werner syndrome
|Disease=Werner syndrome
|CLNACC=RCV000005782.1
|Tags=PM;PMC;SLO;VLD;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1514:C0043119:277700:902:51626007
}}

{{PMID Auto
|PMID=16673358
|Title=The spectrum of WRN mutations in Werner syndrome patients.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}