{{Rsnum
|rsid = 28928903
|Gene = LMNA
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Chromosome=1
|position=156115087
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|desc=WERNER SYNDROME, ATYPICAL
|id=150330
|rsnum=28928903
|variant=0030
}}
{{ neighbor
| rsid = 28928900
| distance = 9
}}

{{ClinVar
|rsid=28928903
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=156115087
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000a05000002110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.156115087G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000015600.22; RCV000057349.1
|CLNDBN=Cardiomyopathy, dilated, with hypergonadotripic hypogonadism; not provided
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|CLNSRCID=NM_005572.3:c.169G>C; LMNA:c.169G>C; 150330.0030
|Disease=Cardiomyopathy; not provided
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}