{{Rsnum
|rsid=61046466
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LMNA
|position=156114934
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=61046466
|variant=0001
}}

{{ClinVar
|rsid=61046466
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=156114934
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000605000002110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.156114934C>T
|CLNSRC=ClinVar; Epithelial Biology; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005572.3:c.16C>T; LMNA:c.16C>T; NBK1674; 150330.0001
|CLNSIG=5
|CLNCUI=C0410190; C0410190
|CLNDBN=Benign scapuloperoneal muscular dystrophy with cardiomyopathy; Primary dilated cardiomyopathy; not provided
|Disease=Benign scapuloperoneal muscular dystrophy with cardiomyopathy; Primary dilated cardiomyopathy; not provided
|CLNACC=RCV000015564.20; RCV000041328.1; RCV000057350.1
|Tags=PM;PMC;SLO;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1436:NBK1674:C0410190:181350:ORPHA261:240072005; NBK1309:C0007193:212110:195021004
}}

{{PMID Auto
|PMID=10080180
|Title=Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.
}}

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