{{Rsnum
|rsid=80338938
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=LMNA
|position=156137756
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=80338938
|variant=0009
}}{{ClinVar
|rsid=80338938
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=156137756
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168080a05000002110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.11:g.156137756C>A; NC_000001.11:g.156137756C>T
|CLNSRC=ClinVar; Epithelial Biology; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1; 0
|CLNSRCID=NM_005572.3:c.1711C>A; NM_170707.3:c.1698+13C>A; LMNA:c.1711C>A; NBK1674; 150330.0009; NM_005572.3:c.1711C>T; NM_170707.3:c.1698+13C>T; LMNA:c.1711C>T
|CLNSIG=5
|CLNCUI=C1449563; C1449563
|CLNDBN=Dilated cardiomyopathy 1A; not provided
|Disease=Dilated cardiomyopathy 1A; not provided
|CLNACC=RCV000015574.24; RCV000057044.1; RCV000057045.1
|Tags=PM;PMC;SLO;NSM;REF;INT;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.
}}