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Gene entry

MYPN

myopalladin

Chromosome
10
Cytoband
10q21.3
Variants (rsID)
58

MYPN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q21.3). Its official name is “myopalladin”. The reference table lists 58 variants (rsID) for this gene.

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Clinically classified variants

28 reference-table entries with clinical significance.

  • rs11596653Benignsingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1KK
  • rs147659164Benignsingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1KK
  • rs2817760Benignsingle nucleotide variantDilated cardiomyopathy 1KK
  • rs7079481Benignsingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1KK|MYPN-related myopathy
  • rs112518450Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1KK
  • rs138313730Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1KK|Cardiovascular phenotype|Primary familial dilated cardiomyopathy|Primary dilated cardiomyopathy|Heart failure|Cardiomyopathy
  • rs140148105Conflicting interpretationssingle nucleotide variantFamilial hypertrophic cardiomyopathy 22|Dilated cardiomyopathy 1KK|Primary dilated cardiomyopathy|Cardiovascular phenotype
  • rs142354704Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1KK
  • rs145142157Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1KK
  • rs149887823Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1KK|Cardiovascular phenotype
  • rs150911078Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Cardiomyopathy|Dilated cardiomyopathy 1KK
  • rs151282801Conflicting interpretationssingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Cardiovascular phenotype|Dilated cardiomyopathy 1KK
  • rs199476401Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1KK|Primary dilated cardiomyopathy
  • rs71534278Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1KK|Familial hypertrophic cardiomyopathy 22|Primary dilated cardiomyopathy|Cardiovascular phenotype|Hypertrophic cardiomyopathy|Cardiomyopathy
  • rs750903219Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1KK
  • rs754227127Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1KK
  • rs138583865Likely benignsingle nucleotide variantDilated cardiomyopathy 1KK
  • rs143574079Likely benignsingle nucleotide variantDilated cardiomyopathy 1KK|Cardiovascular phenotype
  • rs148407539Likely benignsingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1KK
  • rs199585352Likely benignsingle nucleotide variantPrimary dilated cardiomyopathy|Dilated cardiomyopathy 1KK
  • rs140439935Uncertain significancesingle nucleotide variantDilated cardiomyopathy 1KK
  • rs142874859Uncertain significancesingle nucleotide variantDilated cardiomyopathy 1KK
  • rs193022869Uncertain significancesingle nucleotide variantDilated cardiomyopathy 1KK
  • rs199476414Uncertain significancesingle nucleotide variantDilated cardiomyopathy 1KK
  • rs200646285Uncertain significancesingle nucleotide variantDilated cardiomyopathy 1KK
  • rs201693405Uncertain significancesingle nucleotide variantCardiovascular phenotype|Dilated cardiomyopathy 1KK
  • rs71584501Uncertain significancesingle nucleotide variantDilated cardiomyopathy 1KK
  • rs786205457Uncertain significancesingle nucleotide variantHypertrophic cardiomyopathy

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.