{{Rsnum
|rsid=58672172
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LMNA
|position=156136251
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=58672172
|variant=0043
}}

{{ClinVar
|rsid=58672172
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=156136251
|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.156136251C>T
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005572.3:c.1195C>T; LMNA:c.1195C>T; 150330.0043
|CLNSIG=5
|CLNCUI=C1720860
|CLNDBN=Lipodystrophy, familial partial, type 2; not provided
|Disease=Lipodystrophy; not provided
|CLNACC=RCV000015616.24; RCV000057255.1
|Tags=PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1720860:151660:ORPHA2348
}}

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