{{Rsnum
|rsid=113605263
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=TPM3
|position=154167941
|Gene_s=TPM3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=191030
|rsnum=113605263
|variant=0003
}}{{ClinVar
|rsid=113605263
|Reversed=0
|FwdREF=C
|FwdALT=A,G,T
|REF=C
|ALT=A,G,T
|RSPOS=154167941
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168280005000502110104
|GENEINFO=TPM3:7170
|GENE_NAME=TPM3
|GENE_ID=7170
|WGT=1
|VC=SNV
|CLNALLE=3
|CLNHGVS=NC_000001.11:g.154167941C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_152263.3:c.855-1G>A; 191030.0003
|CLNSIG=5
|CLNCUI=C1836448
|CLNDBN=Nemaline myopathy 1
|Disease=Nemaline myopathy 1
|CLNACC=RCV000013261.21
|Tags=PM;PMC;SLO;ASS;INT;ASP;HD;GNO;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1259:NBK1288:C1836448:609284:ORPHA171881:ORPHA607
}}{{PMID Auto
|PMID=12196661
|Title=Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy.
}}