{{Rsnum
|rsid=56699480
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LMNA
|position=156137017
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LMNA
}}{{omim
|id=150330
|rsnum=56699480
|variant=0038
}}

{{ClinVar
|rsid=56699480
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=156137017
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000605000002110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.156137017C>T
|CLNSRC=ClinVar; Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005572.3:c.1477C>T; LMNA:c.1477C>T; 150330.0038
|CLNSIG=5
|CLNCUI=C1834653
|CLNDBN=Limb-girdle muscular dystrophy, type 1B; not provided
|Disease=Limb-girdle muscular dystrophy; not provided
|CLNACC=RCV000015609.20; RCV000057304.1
|Tags=PM;S3D;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}}