{{Rsnum
|rsid=58922911
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=LMNA
|position=156115094
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=58922911
|variant=0054
}}

{{ClinVar
|rsid=58922911
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=156115094
|CHROM=1
|dbSNPBuildID=137
|SSR=0
|SAO=0
|VP=0x050160000a05000002110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.156115094T>G
|CLNSIG=5
|Tags=PM;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000015627.24; RCV000057357.1
|CLNDBN=Cardiomyopathy, dilated, with hypergonadotripic hypogonadism; not provided
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|CLNSRCID=NM_005572.3:c.176T>G; LMNA:c.176T>G; 150330.0052
|Disease=Cardiomyopathy; not provided
|CLNORIGIN=1
}}

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