{{Rsnum
|rsid=137853306
|Chromosome=9
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TPM2
|position=35689265
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TPM2
}}[[Nemaline myopathy]]; NEM4

OMIM 190990.0005
{{omim
|id=190990
|variant=0005
|rsnum=137853306
}}{{ClinVar
|rsid=137853306
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=35689262
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=TPM2:7169
|GENE_NAME=TPM2
|GENE_ID=7169
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.35689262C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=190990.0005
|CLNSIG=5
|CLNCUI=C1836447
|CLNDBN=Nemaline myopathy 4
|Disease=Nemaline myopathy 4
|CLNACC=RCV000013280.22
|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=17846275
|Title=Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2).
}}

{{PMID Auto
|PMID=18422639
|Title=Beta-tropomyosin mutations alter tropomyosin isoform composition.
}}