{{Rsnum
|rsid=60864230
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=LMNA
|position=156130658
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=60864230
|variant=0027
}}
{{omim
|id=150330
|rsnum=60864230
|variant=0032
}}

{{ClinVar
|rsid=60864230
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=156130658
|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.156130658G>C; NC_000001.11:g.156130658G>T
|CLNORIGIN=1
|CLNSRCID=
NM_005572.3:c.398G>C; LMNA:c.398G>C; 150330.0032; NM_005572.3:c.398G>T; LMNA:c.398G>T; 150330.0027
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000015602.24; RCV000057398.1; RCV000015577.26; RCV000015578.26; RCV000057399.1
|Tags=PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDBN=Benign scapuloperoneal muscular dystrophy with cardiomyopathy; not provided; Lipodystrophy, familial partial, type 2; Hutchinson-gilford progeria syndrome, childhood-onset
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1436:NBK1674:C0410190:181350:ORPHA261:240072005; C1720860:151660:ORPHA2348; CN070028
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|Disease=Benign scapuloperoneal muscular dystrophy with cardiomyopathy; not provided; Lipodystrophy; Hutchinson-gilford progeria syndrome
}}

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