{{Rsnum
|rsid=121912496
|Chromosome=1
|position=156134910
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LMNA
|Gene_s=LMNA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=150330
|rsnum=121912496
|variant=0048
}}{{ClinVar
|rsid=121912496
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=156134910
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000a05000002110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.11:g.156134910C>G; NC_000001.11:g.156134910C>T
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005572.3:c.745C>G; NM_005572.3:c.745C>T; LMNA:c.745C>T; 150330.0048
|CLNSIG=5
|CLNCUI=C2750785
|CLNDBN=Myopathy; Congenital muscular dystrophy, LMNA-related; not provided
|Disease=Myopathy; Congenital muscular dystrophy; not provided
|CLNACC=RCV000041362.1; RCV000015621.24; RCV000057452.1
|Tags=PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C0026848; NBK1291:C2750785:613205:ORPHA157973
}}