{{Rsnum
|rsid=199476153
|Chromosome=9
|position=35685509
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GAG)
|geno3=(GAG;GAG)
|Gene=TPM2
|Gene_s=TPM2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=T
|CHROM=9
|CLNACC=RCV000013281.23
|CLNALLE=1
|CLNDBN=Cap myopathy 2
|CLNHGVS=NC_000009.11:g.35685506_35685508delCTC
|CLNORIGIN=33
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=190990.0006
|Disease=Cap myopathy 2
|FwdREF=GAG
|GENEINFO=TPM2:7169
|GENE_ID=7169
|GENE_NAME=TPM2
|REF=TCTC
|RSPOS=35685505
|Reversed=1
|SAO=3
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=199476153
|CLNDSDB=MedGen
|CLNDSDBID=CN178537
}}{{PMID Auto
|PMID=17434307
|Title=Cap disease caused by heterozygous deletion of the beta-tropomyosin gene TPM2.
}}

{{PMID Auto
|PMID=19345583
|Title=Cap disease due to mutation of the beta-tropomyosin gene (TPM2).
}}