{{Rsnum
|rsid=121908447
|Chromosome=8
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=WRN
|position=31147397
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WRN
}}{{omim
|id=604611
|rsnum=121908447
|variant=0002
}}{{ClinVar
|rsid=121908447
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=31004913
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=WRN:7486
|GENE_NAME=WRN
|GENE_ID=7486
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.31004913C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604611.0002
|CLNSIG=5
|CLNCUI=C0043119
|CLNDBN=Werner syndrome
|Disease=Werner syndrome
|CLNACC=RCV000005778.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1514:C0043119:277700:902:51626007
}}