{{Rsnum
|rsid=58048078
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=LMNA
|position=156134942
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=58048078
|variant=0035
}}

{{ClinVar
|rsid=58048078
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=156134942
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000605000002110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.156134942T>A
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005572.3:c.777T>A; LMNA:c.777T>A; 150330.0035
|CLNSIG=5
|CLNCUI=C1834653
|CLNDBN=Limb-girdle muscular dystrophy, type 1B; not provided
|Disease=Limb-girdle muscular dystrophy; not provided
|CLNACC=RCV000015605.20; RCV000057457.1
|Tags=PM;SLO;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1291:C1834653:159001:ORPHA264
}}

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