{{Rsnum
|rsid = 28933091
|Gene = LMNA
|geno1 = (C;C)
|geno2 = (C;G)
|geno3 = (G;G)
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=G
|Chromosome=1
|position=156134474
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|desc=CARDIOMYOPATHY, DILATED, 1A
|id=150330
|rsnum=28933091
|variant=0007
}}{{ClinVar
|rsid=28933091
|Reversed=0
|FwdREF=C
|FwdALT=A,G
|REF=C
|ALT=A,G
|RSPOS=156134474
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000a05000002110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.11:g.156134474C>A; NC_000001.11:g.156134474C>G
|CLNSRC=ClinVar; Epithelial Biology; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0; 1
|CLNSRCID=NM_005572.3:c.585C>A; LMNA:c.585C>A; NM_005572.3:c.585C>G; LMNA:c.585C>G; NBK1674; 150330.0007
|CLNSIG=5
|CLNCUI=C1449563; C1449563
|CLNDBN=not provided; Dilated cardiomyopathy 1A
|Disease=not provided; Dilated cardiomyopathy 1A
|CLNACC=RCV000057424.1; RCV000015572.25; RCV000057425.1
|Tags=PM;PMC;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1674:C1449563:115200
}}{{PMID Auto
|PMID=10580070
|Title=Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.
}}