{{Rsnum
|rsid=11575937
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LMNA
|position=156136985
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=11575937
|variant=0010
}}
{{omim
|id=150330
|rsnum=11575937
|variant=0012
}}{{ClinVar
|rsid=11575937
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=156136985
|CHROM=1
|dbSNPBuildID=120
|SSR=0
|SAO=1
|VP=0x050360000a05000102110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.11:g.156136985G>A; NC_000001.11:g.156136985G>T
|CLNORIGIN=1
|CLNSRCID=
NM_005572.3:c.1445G>A; LMNA:c.1445G>A; 150330.0010; NM_005572.3:c.1445G>T; LMNA:c.1445G>T; 150330.0012
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000015575.24; RCV000041318.1; RCV000057299.1; RCV000015580.24; RCV000057300.1
|Tags=PM;S3D;SLO;NSM;REF;ASP;GNO;OTHERKG;LSD;OM
|CLNDBN=Lipodystrophy, familial partial, type 2; Primary dilated cardiomyopathy; not provided
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C1720860:151660:ORPHA2348; NBK1309:C0007193:212110:195021004
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|Disease=Lipodystrophy; Primary dilated cardiomyopathy; not provided
}}