{{Rsnum
|rsid=121912495
|Chromosome=1
|position=156136103
|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=121912495
|variant=0047
}}{{ClinVar
|rsid=121912495
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=156136103
|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
|CLNHGVS=NC_000001.11:g.156136103T>C
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005572.3:c.1139T>C; LMNA:c.1139T>C; 150330.0047
|CLNSIG=5
|CLNCUI=C2750785
|CLNDBN=Congenital muscular dystrophy, LMNA-related; not provided
|Disease=Congenital muscular dystrophy; not provided
|CLNACC=RCV000015620.24; RCV000057237.1
|Tags=PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1291:C2750785:613205:ORPHA157973
}}