{{Rsnum
|rsid=137853307
|Chromosome=9
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=TPM2
|position=35684765
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TPM2
}}[[Nemaline myopathy]]; NEM4

OMIM 190990.0008
{{omim
|id=190990
|variant=0008
|rsnum=137853307
}}{{ClinVar
|rsid=137853307
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=35684762
|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.35684762G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000013283.16
|CLNDBN=Cap myopathy 2
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=190990.0008
|Disease=Cap myopathy 2
|CLNDSDB=MedGen
|CLNDSDBID=CN178537
}}{{PMID Auto
|PMID=19047562
|Title=New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations.
}}