{{Rsnum
|rsid=199474724
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LMNA
|position=156134839
|Gene_s=LMNA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000034134.2
|CLNALLE=1
|CLNDBN=Benign scapuloperoneal muscular dystrophy with cardiomyopathy
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1436:NBK1674:C0410190:181350:ORPHA261:240072005
|CLNHGVS=NC_000001.11:g.156134839G>A
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=ClinVar; GeneReviews
|CLNSRCID=NM_005572.3:c.674G>A; NBK1436
|Disease=Benign scapuloperoneal muscular dystrophy with cardiomyopathy
|FwdALT=A
|FwdREF=G
|GENEINFO=LMNA:4000
|GENE_ID=4000
|GENE_NAME=LMNA
|REF=G
|RSPOS=156134839
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000a05000002110100
|WGT=1
|dbSNPBuildID=136
|rsid=199474724
}}{{PMID Auto
|PMID=22431096
|Title=Autosomal recessive Emery-Dreifuss muscular dystrophy caused by a novel mutation (R225Q) in the lamin A/C gene identified by exome sequencing.
}}