{{Rsnum
|rsid=57520892
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=LMNA
|position=156137204
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=57520892
|variant=0003
}}
{{omim
|id=150330
|rsnum=57520892
|variant=0021
}}

{{ClinVar
|rsid=57520892
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=156137204
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000a05000002110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.11:g.156137204G>A; NC_000001.11:g.156137204G>C
|CLNORIGIN=1
|CLNSRCID=
NM_005572.3:c.1580G>A; LMNA:c.1580G>A; 150330.0021; NM_005572.3:c.1580G>C; LMNA:c.1580G>C; 150330.0003
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000015591.24; RCV000015592.24; RCV000057326.1; RCV000015569.24; RCV000015570.20; RCV000057327.1
|Tags=PM;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDBN=Mandibuloacral dysostosis; MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL; not provided; Benign scapuloperoneal muscular dystrophy with cardiomyopathy; Lipodystrophy, familial partial, type 2
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=C0432291:248370:ORPHA2457:109419009; C2673440; NBK1436:NBK1674:C0410190:181350:ORPHA261:240072005; C1720860:151660:ORPHA2348
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|Disease=Mandibuloacral dysostosis; MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; not provided; Benign scapuloperoneal muscular dystrophy with cardiomyopathy; Lipodystrophy
}}

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