{{Rsnum
|rsid=58932704
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LMNA
|position=156136413
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=58932704
|variant=0002
}}

{{ClinVar
|rsid=58932704
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=156136413
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000a05000002110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.156136413C>T
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005572.3:c.1357C>T; LMNA:c.1357C>T; 150330.0002
|CLNSIG=5
|CLNCUI=C0410190
|CLNDBN=Benign scapuloperoneal muscular dystrophy with cardiomyopathy; not provided
|Disease=Benign scapuloperoneal muscular dystrophy with cardiomyopathy; not provided
|CLNACC=RCV000015565.24; RCV000057273.1
|Tags=PM;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1436:NBK1674:C0410190:181350:ORPHA261:240072005
}}

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