{{Rsnum
|rsid=267607008
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=WRN
|position=31064962
|Gene_s=WRN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=8
|CLNACC=RCV000005786.1
|CLNALLE=1
|CLNDBN=Werner syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1514:C0043119:277700:902:51626007
|CLNHGVS=NC_000008.10:g.30922478A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604611.0010
|Disease=Werner syndrome
|FwdALT=G
|FwdREF=A
|GENEINFO=WRN:7486
|GENE_ID=7486
|GENE_NAME=WRN
|REF=A
|RSPOS=30922478
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607008
}}