{{Rsnum
|rsid=58596362
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LMNA
|position=156138613
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=58596362
|variant=0022
}}

{{ClinVar
|rsid=58596362
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=156138613
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160080305000002110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.156138613C>T
|CLNSRC=ClinVar; Emory University; Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001282626.1:c.1818+6C>T; NM_170707.3:c.1824C>T; 3566; LMNA:c.1824C>T; 150330.0022
|CLNSIG=5
|CLNCUI=C0033300; C0406585
|CLNDBN=Hutchinson-Gilford syndrome; Lethal tight skin contracture syndrome; not provided
|Disease=Hutchinson-Gilford syndrome; Lethal tight skin contracture syndrome; not provided
|CLNACC=RCV000015593.24; RCV000015594.24; RCV000057364.2
|Tags=PM;SLO;REF;SYN;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1121:C0033300:176670:ORPHA740:238870004; C0406585:275210:ORPHA1662:400128006
}}

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