{{Rsnum
|rsid=60310264
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LMNA
|position=156130693
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=60310264
|variant=0024
}}{{ClinVar
|rsid=60310264
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=156130693
|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.156130693G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000015596.20; RCV000057406.1
|CLNDBN=Hutchinson-Gilford progeria syndrome, atypical; not provided
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|CLNSRCID=NM_005572.3:c.433G>A; LMNA:c.433G>A; 150330.0024
|Disease=Hutchinson-Gilford progeria syndrome; not provided
}}