{{Rsnum
|rsid=60890628
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LMNA
|position=156138507
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=60890628
|variant=0041
}}

{{ClinVar
|rsid=60890628
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=156138507
|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.156138507C>T
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_170707.3:c.1718C>T; LMNA:c.1718C>T; 150330.0041
|CLNSIG=5
|CLNCUI=C1449563; C1720860
|CLNDBN=Dilated cardiomyopathy 1A; MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL; Lipodystrophy, familial partial, type 2; AllHighlyPenetrant; not provided
|Disease=Dilated cardiomyopathy 1A; MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; Lipodystrophy; AllHighlyPenetrant; not provided
|CLNACC=RCV000015612.24; RCV000015613.24; RCV000015614.20; RCV000041329.1; RCV000057351.1
|Tags=PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; MedGen; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1674:C1449563:115200; C2673440; C1720860:151660:ORPHA2348; CN169374
}}

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