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Gene entry

AKAP9

A-kinase anchoring protein 9

Chromosome
7
Cytoband
7q21.2
Variants (rsID)
71

AKAP9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q21.2). Its official name is “A-kinase anchoring protein 9”. The reference table lists 71 variants (rsID) for this gene.

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Clinically classified variants

50 reference-table entries with clinical significance.

  • rs139963188Benignsingle nucleotide variantLong QT syndrome|Long QT syndrome 11
  • rs142401936Benignsingle nucleotide variantLong QT syndrome 11|Cardiovascular phenotype|Long QT syndrome
  • rs149946443Benignsingle nucleotide variantCardiovascular phenotype|Long QT syndrome 11|Restrictive cardiomyopathy|Long QT syndrome
  • rs150016098Benignsingle nucleotide variantCardiovascular phenotype|Long QT syndrome 11|unspecified heart condition|Long QT syndrome
  • rs186148498Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Long QT syndrome 11
  • rs2230768Benignsingle nucleotide variantLong QT syndrome|Congenital long QT syndrome|Cardiovascular phenotype|Long QT syndrome 11
  • rs34101758Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Long QT syndrome 11
  • rs34327395Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Congenital long QT syndrome|Long QT syndrome 11|Cardiomyopathy
  • rs34956633Benignsingle nucleotide variantCardiovascular phenotype|Congenital long QT syndrome|Long QT syndrome|Long QT syndrome 11
  • rs35759833Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Congenital long QT syndrome|Long QT syndrome 11
  • rs61757673Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiomyopathy|Ventricular fibrillation|Long QT syndrome 11
  • rs6964587Benignsingle nucleotide variantColorectal cancer|Cardiovascular phenotype|Long QT syndrome|Long QT syndrome 11
  • rs139046510Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Long QT syndrome|Congenital long QT syndrome|Long QT syndrome 11
  • rs139468199Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiovascular phenotype
  • rs139612565Conflicting interpretationssingle nucleotide variantCongenital long QT syndrome|Cardiovascular phenotype|Long QT syndrome
  • rs139770404Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Congenital long QT syndrome|Long QT syndrome 11
  • rs140470576Conflicting interpretationssingle nucleotide variantLong QT syndrome|Congenital long QT syndrome|Cardiovascular phenotype|Long QT syndrome 11
  • rs141039834Conflicting interpretationssingle nucleotide variantLong QT syndrome|Congenital long QT syndrome|Cardiovascular phenotype|Ventricular tachycardia
  • rs142573103Conflicting interpretationssingle nucleotide variantLong QT syndrome
  • rs144054367Conflicting interpretationssingle nucleotide variantArrhythmogenic right ventricular cardiomyopathy|Congenital long QT syndrome|Long QT syndrome|Cardiovascular phenotype
  • rs144875383Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Long QT syndrome|Long QT syndrome 11
  • rs144888041Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Congenital long QT syndrome|Brugada syndrome 1|Long QT syndrome 11|Catecholaminergic polymorphic ventricular tachycardia
  • rs146710448Conflicting interpretationssingle nucleotide variantLong QT syndrome|Congenital long QT syndrome|Cardiovascular phenotype
  • rs150332727Conflicting interpretationssingle nucleotide variantCongenital long QT syndrome|Cardiovascular phenotype|Long QT syndrome
  • rs151021935Conflicting interpretationssingle nucleotide variantSudden cardiac death|Long QT syndrome|Congenital long QT syndrome|Cardiovascular phenotype|Long QT syndrome 11
  • rs189083857Conflicting interpretationssingle nucleotide variantLong QT syndrome
  • rs193922723Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiac arrhythmia
  • rs200327385Conflicting interpretationssingle nucleotide variantLong QT syndrome|Congenital long QT syndrome
  • rs200844952Conflicting interpretationssingle nucleotide variantLong QT syndrome|Congenital long QT syndrome|Cardiovascular phenotype
  • rs201048693Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiomyopathy|Cardiovascular phenotype|Long QT syndrome 11
  • rs201977551Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Congenital long QT syndrome
  • rs367857951Conflicting interpretationssingle nucleotide variantCongenital long QT syndrome|Long QT syndrome|Cardiovascular phenotype
  • rs534185372Conflicting interpretationssingle nucleotide variantCongenital long QT syndrome|Long QT syndrome|Cardiovascular phenotype
  • rs553800160Conflicting interpretationssingle nucleotide variantLong QT syndrome
  • rs56198613Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Long QT syndrome 11|Long QT syndrome
  • rs61757557Conflicting interpretationssingle nucleotide variantCongenital long QT syndrome|Cardiovascular phenotype|Long QT syndrome
  • rs61757664Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Long QT syndrome 11|Congenital long QT syndrome|Long QT syndrome
  • rs61757671Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Congenital long QT syndrome|Long QT syndrome|Long QT syndrome 11
  • rs73226383Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Congenital long QT syndrome|Long QT syndrome 11
  • rs755408339Conflicting interpretationssingle nucleotide variantCongenital long QT syndrome
  • rs756398963Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Long QT syndrome|Congenital long QT syndrome
  • rs775991910Conflicting interpretationssingle nucleotide variantCongenital long QT syndrome|Long QT syndrome
  • rs80191629Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Congenital long QT syndrome
  • rs150379637Likely benignsingle nucleotide variantCardiovascular phenotype|Long QT syndrome
  • rs184184931Likely benignsingle nucleotide variantCardiovascular phenotype|Long QT syndrome
  • rs185898118Likely benignsingle nucleotide variantLong QT syndrome
  • rs187255726Likely benignsingle nucleotide variantLong QT syndrome
  • rs61757663Likely benignsingle nucleotide variantLong QT syndrome 11|Long QT syndrome
  • rs150579291Uncertain significancesingle nucleotide variantCardiovascular phenotype|Long QT syndrome
  • rs201545032Uncertain significancesingle nucleotide variantLong QT syndrome

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.