{{Rsnum
|rsid=104894129
|Chromosome=9
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TPM2
|position=35685672
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TPM2
}}{{omim
|id=190990
|rsnum=104894129
|variant=0003
}}{{ClinVar
|rsid=104894129
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=35685669
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=3
|VP=0x050368000000000002110100
|GENEINFO=TPM2:7169
|GENE_NAME=TPM2
|GENE_ID=7169
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.35685669C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1259; 190990.0003
|CLNSIG=5
|CLNCUI=C1836447
|CLNDBN=Nemaline myopathy 4
|Disease=Nemaline myopathy 4
|CLNACC=RCV000013278.16
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1259:NBK1288:C1836447:609285:171881:607
}}{{PMID Auto
|PMID=11738357
|Title=Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy.
}}{{PMID Auto
|PMID=18789687
|Title=TPM2 mutation.
}}