{{Rsnum
|rsid=104894502
|Chromosome=15
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TPM1
|position=63060915
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TPM1
}}see [[rs28934269]], an equivalent SNP

{{omim
|id=191010
|rsnum=104894502
|variant=0001
}}{{ClinVar
|rsid=104894502
|Reversed=0
|FwdREF=A
|FwdALT=G,T
|REF=A
|ALT=G,T
|RSPOS=63353114
|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.63353114A>G; NC_000015.9:g.63353114A>T
|CLNORIGIN=1
|CLNSRCID=
TPM1_00010; 191010.0001; TPM1_00011
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000013271.23; RCV000024576.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=Familial hypertrophic cardiomyopathy 3; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1768:C1861863:115196
|CLNSRC=Leiden Muscular Dystrophy pages (TPM1); OMIM Allelic Variant
|Disease=Familial hypertrophic cardiomyopathy 3; not provided
}}{{PMID Auto
|PMID=8205619
|Title=Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.
}}

{{PMID Auto
|PMID=11603924
|Title=A familial hypertrophic cardiomyopathy alpha-tropomyosin mutation causes severe cardiac hypertrophy and death in mice.
}}

{{PMID Auto
|PMID=11044437
|Title=Novel mutation in the alpha-tropomyosin gene and transition from hypertrophic to hypocontractile dilated cardiomyopathy.
}}