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Gene entry

BAG3

BAG cochaperone 3

Chromosome
10
Cytoband
10q26.11
Variants (rsID)
33

BAG3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q26.11). Its official name is “BAG cochaperone 3”. The reference table lists 33 variants (rsID) for this gene.

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Clinically classified variants

27 reference-table entries with clinical significance.

  • rs11199065Benignsingle nucleotide variantDilated cardiomyopathy 1HH|Myofibrillar myopathy 6
  • rs117671123Benignsingle nucleotide variantMyofibrillar myopathy|Myofibrillar myopathy 6|Cardiovascular phenotype|Myofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Dilated cardiomyopathy 1HH
  • rs2234962Benignsingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6
  • rs35434411Benignsingle nucleotide variantDilated cardiomyopathy 1HH|Myofibrillar myopathy 6|Cardiovascular phenotype|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6
  • rs117749531Conflicting interpretationssingle nucleotide variantMyofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6|Dilated cardiomyopathy 1HH
  • rs138832242Conflicting interpretationssingle nucleotide variantMyofibrillar myopathy 6|Dilated cardiomyopathy 1HH
  • rs141355480Conflicting interpretationssingle nucleotide variantMyofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Cardiomyopathy
  • rs143919208Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1HH|Myofibrillar myopathy 6
  • rs144678100Conflicting interpretationssingle nucleotide variantMyofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Cardiovascular phenotype
  • rs145393807Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Primary dilated cardiomyopathy|Myofibrillar myopathy 6|Myofibrillar myopathy 6|Dilated cardiomyopathy 1HH
  • rs147259596Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1HH|Myofibrillar myopathy 6|Myofibrillar myopathy 6|Dilated cardiomyopathy 1HH
  • rs201638005Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Left ventricular noncompaction|Myofibrillar myopathy 6|Dilated cardiomyopathy 1HH
  • rs34656239Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1HH|Myofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6
  • rs375257731Conflicting interpretationssingle nucleotide variantMyofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6
  • rs376198104Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1HH|Myofibrillar myopathy 6
  • rs387906874Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1HH|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6|Primary dilated cardiomyopathy
  • rs397516882Conflicting interpretationssingle nucleotide variantMyofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6
  • rs556465096Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1HH|Myofibrillar myopathy 6|Myofibrillar myopathy 6|Dilated cardiomyopathy 1HH
  • rs775151738Conflicting interpretationssingle nucleotide variantMyofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6
  • rs397514507Likely pathogenicsingle nucleotide variantDilated cardiomyopathy 1HH
  • rs1057517945Pathogenicsingle nucleotide variantDilated cardiomyopathy 1HH|Myofibrillar myopathy 6
  • rs121918312Pathogenicsingle nucleotide variantMyofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6|Peripheral neuropathy
  • rs397516881Pathogenicsingle nucleotide variantPrimary dilated cardiomyopathy|Dilated cardiomyopathy 1HH|Myofibrillar myopathy 6
  • rs727505109PathogenicDeletionPrimary dilated cardiomyopathy|Myofibrillar myopathy 6|Dilated cardiomyopathy 1HH
  • rs794728981PathogenicDeletionInborn genetic diseases
  • rs869248137Pathogenicsingle nucleotide variantPrimary dilated cardiomyopathy|Myofibrillar myopathy 6|Dilated cardiomyopathy 1HH|Primary familial dilated cardiomyopathy|Primary dilated cardiomyopathy|Myocarditis
  • rs876661342Pathogenicsingle nucleotide variantMyofibrillar myopathy 6|Dilated cardiomyopathy 1HH

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.