{{Rsnum
|rsid=199476315
|Chromosome=15
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TPM1
|position=63061723
|Gene_s=TPM1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=15
|CLNACC=RCV000024578.1; RCV000036627.1; RCV000054795.23
|CLNALLE=1
|CLNDBN=not provided; Primary familial hypertrophic cardiomyopathy; Left ventricular noncompaction 9
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen
|CLNDSDBID=NBK1768:C0949658:83978005; CN179850
|CLNHGVS=NC_000015.9:g.63353922G>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=Leiden Muscular Dystrophy pages (TPM1); OMIM Allelic Variant
|CLNSRCID=TPM1_00013; 191010.0007
|Disease=not provided; Primary familial hypertrophic cardiomyopathy; Left ventricular noncompaction 9
|FwdALT=A
|FwdREF=G
|GENEINFO=TPM1:7168
|GENE_ID=7168
|GENE_NAME=TPM1
|REF=G
|RSPOS=63353922
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199476315
}}{{PMID Auto
|PMID=12858563
|Title=Molecular epidemiology of hypertrophic cardiomyopathy.
}}

{{PMID Auto
|PMID=21551322
|Title=Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
}}