{{Rsnum
|rsid=60652225
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=LMNA
|position=156130679
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=60652225
|variant=0031
}}

{{ClinVar
|rsid=60652225
|Reversed=0
|FwdREF=T
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=156130679
|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; 2
|CLNHGVS=NC_000001.11:g.156130679T>C; NC_000001.11:g.156130679T>G
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=0; 1
|CLNSRCID=NM_005572.3:c.419T>C; LMNA:c.419T>C; NM_005572.3:c.419T>G; LMNA:c.419T>G; 150330.0031
|CLNSIG=5
|CLNCUI=CN070028
|CLNDBN=not provided; Hutchinson-gilford progeria syndrome, childhood-onset
|Disease=not provided; Hutchinson-gilford progeria syndrome
|CLNACC=RCV000057402.1; RCV000015601.22; RCV000057403.1
|Tags=PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=CN070028
}}

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