{{Rsnum
|rsid=104894501
|Chromosome=15
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TPM1
|position=63044030
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TPM1
}}{{omim
|id=191010
|rsnum=104894501
|variant=0005
}}{{ClinVar
|rsid=104894501
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=63336229
|CHROM=15
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=TPM1:7168
|GENE_NAME=TPM1
|GENE_ID=7168
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000015.9:g.63336229G>A; NC_000015.9:g.63336229G>T
|CLNSRC=Leiden Muscular Dystrophy pages (TPM1); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=TPM1_00001; 191010.0005
|CLNSIG=5
|CLNCUI=C2678476
|CLNDBN=Dilated cardiomyopathy 1Y; AllHighlyPenetrant
|Disease=Dilated cardiomyopathy 1Y; AllHighlyPenetrant
|CLNACC=RCV000013275.15; RCV000036315.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet; MedGen
|CLNDSDBID=NBK1309:C2678476:611878:154:54260; CN169374
}}{{PMID Auto
|PMID=11273725
|Title=Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy.
}}