{{Rsnum
|rsid=60458016
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LMNA
|position=156136036
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=60458016
|variant=0049
}}

{{ClinVar
|rsid=60458016
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=156136036
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000e05000002110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.11:g.156136036G>A; NC_000001.11:g.156136036G>T
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1; 0
|CLNSRCID=NM_005572.3:c.1072G>A; LMNA:c.1072G>A; 150330.0049; NM_005572.3:c.1072G>T; LMNA:c.1072G>T
|CLNSIG=5
|CLNCUI=C0410190; C2750785; C1834653
|CLNDBN=Benign scapuloperoneal muscular dystrophy with cardiomyopathy; Congenital muscular dystrophy, LMNA-related; Limb-girdle muscular dystrophy, type 1B; not provided
|Disease=Benign scapuloperoneal muscular dystrophy with cardiomyopathy; Congenital muscular dystrophy; Limb-girdle muscular dystrophy; not provided
|CLNACC=RCV000015622.24; RCV000015623.24; RCV000015624.24; RCV000057227.1; RCV000057228.1
|Tags=PM;SLO;NSM;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1436:NBK1674:C0410190:181350:ORPHA261:240072005; NBK1291:C2750785:613205:ORPHA157973; NBK1291:C1834653:159001:ORPHA264
}}

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