{{Rsnum
|rsid=4641
|Gene=LMNA
|Chromosome=1
|position=156137743
|Orientation=plus
|GMAF=0.2057
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=LMNA
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 53.6 | 41.1 | 5.4
| HCB | 49.3 | 40.4 | 10.3
| JPT | 59.3 | 35.4 | 5.3
| YRI | 87.0 | 11.6 | 1.4
| ASW | 82.5 | 17.5 | 0.0
| CHB | 49.3 | 40.4 | 10.3
| CHD | 48.6 | 38.5 | 12.8
| GIH | 49.5 | 36.6 | 13.9
| LWK | 90.0 | 10.0 | 0.0
| MEX | 56.1 | 38.6 | 5.3
| MKK | 90.4 | 9.6 | 0.0
| TSI | 61.8 | 33.3 | 4.9
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19841875
|Title=Polymorphisms of the lamina maturation pathway and their association with the metabolic syndrome: the DESIR prospective study
}}

{{ClinVar
|rsid=4641
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=156137743
|CHROM=1
|GMAF=0.2056
|dbSNPBuildID=52
|SSR=0
|SAO=1
|VP=0x05016800000015051f110100
|GENEINFO=LMNA:4000
|GENE_NAME=LMNA
|GENE_ID=4000
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.156137743C>T
|CLNORIGIN=1
|CLNSIG=2
|Tags=PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.7943; 0.2057
|CLNACC=RCV000041327.2; RCV000057348.2
|CLNDBN=AllHighlyPenetrant; not provided
|CLNDSDB=MedGen
|CLNDSDBID=CN169374
|COMMON=1
|Disease=AllHighlyPenetrant; not provided
|CLNSRC=ClinVar; Emory University; Epithelial Biology
|CLNSRCID=NM_005572.3:c.1698C>T; NM_170708.3:c.1608+511C>T; 3474; 3899; LMNA:c.1698C>T
}}

{{PMID Auto
|PMID=15637659
|Title=Linkage disequilibrium patterns and tagSNP transferability among European populations.
|OA=1
}}

{{PMID Auto
|PMID=16262891
|Title=Aging syndrome genes and premature coronary artery disease.
|OA=1
}}

{{PMID Auto
|PMID=17327437
|Title=Common variation in LMNA increases susceptibility to type 2 diabetes and associates with elevated fasting glycemia and estimates of body fat and height in the general population: studies of 7,495 Danish whites.
}}

{{PMID Auto
|PMID=17327460
|Title=Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects.
|OA=1
}}

{{PMID Auto
|PMID=17327461
|Title=Lamin A/C polymorphisms, type 2 diabetes, and the metabolic syndrome: case-control and quantitative trait studies.
|OA=1
}}

{{PMID Auto
|PMID=17994215
|Title=Evaluating the association of common LMNA variants with type 2 diabetes and quantitative metabolic phenotypes in French Europids.
}}

{{PMID Auto
|PMID=20501691
|Title=LMNA rs4641 and the muscle lamin A and C isoforms in twins--metabolic implications and transcriptional regulation.
}}

{{PMID Auto
|PMID=24831476
|Title=[Association between LMNA mutation and familial and idiopathic dilated cardiomyopathy patients in Xinjiang]
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}