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Gene entry

VCL

vinculin

Chromosome
10
Cytoband
10q22.2
Variants (rsID)
37

VCL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q22.2). Its official name is “vinculin”. The reference table lists 37 variants (rsID) for this gene.

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Clinically classified variants

24 reference-table entries with clinical significance.

  • rs137877092Benignsingle nucleotide variantCardiovascular phenotype|Cardiomyopathy|Dilated cardiomyopathy 1W
  • rs7904077Benignsingle nucleotide variantDilated cardiomyopathy 1W|Cardiomyopathy
  • rs140381835Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1W
  • rs141033098Conflicting interpretationssingle nucleotide variantCardiomyopathy|Cardiovascular phenotype|Primary familial dilated cardiomyopathy|Ventricular tachycardia|Dilated cardiomyopathy 1W
  • rs143702799Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1W|Cardiovascular phenotype
  • rs148966602Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1W|Cardiomyopathy
  • rs150385900Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1W|Cardiomyopathy
  • rs183739128Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1W|Cardiovascular phenotype
  • rs189242810Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Cardiomyopathy|Dilated cardiomyopathy 1W
  • rs189781480Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1W
  • rs200342284Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1W|Cardiomyopathy|Primary dilated cardiomyopathy
  • rs201528612Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1W|Hypertrophic cardiomyopathy 15|Dilated cardiomyopathy 1W
  • rs367598954Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1W
  • rs368570586Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1W
  • rs397517244Conflicting interpretationssingle nucleotide variantPrimary dilated cardiomyopathy|Dilated cardiomyopathy 1W
  • rs532645343Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1W
  • rs576271894Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1W|Cardiovascular phenotype|Cardiomyopathy
  • rs71579374Conflicting interpretationssingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Cardiovascular phenotype|Dilated cardiomyopathy 1W|Primary dilated cardiomyopathy
  • rs71579375Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Cardiomyopathy|Primary familial dilated cardiomyopathy|Dilated cardiomyopathy 1W
  • rs71579379Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1W|Cardiomyopathy|Primary dilated cardiomyopathy
  • rs775062250Conflicting interpretationssingle nucleotide variantDilated Cardiomyopathy, Dominant|Dilated cardiomyopathy 1W
  • rs781036800Conflicting interpretationsDeletionPrimary dilated cardiomyopathy|Hypertrophic cardiomyopathy 15|Dilated cardiomyopathy 1W
  • rs146278697Likely benignsingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1W
  • rs145393322Uncertain significancesingle nucleotide variantDilated cardiomyopathy 1W

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.