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Gene entry

ANK2

ankyrin 2

Chromosome
4
Cytoband
4q25-q26
Variants (rsID)
218

ANK2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q25-q26). Its official name is “ankyrin 2”. The reference table lists 218 variants (rsID) for this gene.

Clinically classified variants

55 reference-table entries with clinical significance.

  • rs116128106Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs138641014Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs138842207Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs140926982Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs142159132Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs142908806Benignsingle nucleotide variantLong QT syndrome|Cardiac arrhythmia, ankyrin-B-related|Cardiovascular phenotype
  • rs143161930Benignsingle nucleotide variantLong QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs145895389Benignsingle nucleotide variantCardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related|Long QT syndrome
  • rs147423696Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs150226540Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs150878494Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs201645638Benignsingle nucleotide variantLong QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs34270799Benignsingle nucleotide variantCardiovascular phenotype|Long QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs35249198Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs35530544Benignsingle nucleotide variantCardiac arrhythmia, ankyrin-B-related|Long QT syndrome|Cardiovascular phenotype|Cardiomyopathy|Cardiac arrhythmia
  • rs36210417Benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related|Cardiomyopathy|Atrial fibrillation
  • rs3733617Benignsingle nucleotide variantCardiovascular phenotype|Long QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs45454496Benignsingle nucleotide variantCardiac arrhythmia, ankyrin-B-related|Cardiovascular phenotype|Ventricular fibrillation|Long QT syndrome|Cardiac arrhythmia
  • rs121912705Conflicting interpretationssingle nucleotide variantCardiac arrhythmia, ankyrin-B-related|Long QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia
  • rs121912706Conflicting interpretationssingle nucleotide variantLong QT syndrome 4|Death in infancy|Cardiovascular phenotype|Cardiomyopathy|Long QT syndrome|Cardiac arrhythmia, ankyrin-B-related|Cardiac arrhythmia
  • rs140606121Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiovascular phenotype
  • rs144158934Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs144848998Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs146964054Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs148462839Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs148851013Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs150684838Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiomyopathy
  • rs193922637Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiac arrhythmia
  • rs29372Conflicting interpretationssingle nucleotide variantCardiac arrhythmia, ankyrin-B-related|Long QT syndrome
  • rs34591340Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Long QT syndrome|Cardiomyopathy|Hypertrophic cardiomyopathy|Cardiac arrhythmia, ankyrin-B-related
  • rs372870729Conflicting interpretationssingle nucleotide variantCardiac arrhythmia, ankyrin-B-related
  • rs374884110Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs377608305Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Long QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs45570339Conflicting interpretationssingle nucleotide variantCongenital long QT syndrome|Long QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs45602336Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Long QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs528909081Conflicting interpretationssingle nucleotide variantLong QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs66785829Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Familial dilated cardiomyopathy and peripheral neuropathy|Long QT syndrome|Cardiac arrhythmia, ankyrin-B-related|Conduction disorder of the heart|Cardiac arrhythmia
  • rs72544141Conflicting interpretationssingle nucleotide variantLong QT syndrome 4|Cardiac arrhythmia, ankyrin-B-related|Congenital long QT syndrome|Long QT syndrome|Cardiovascular phenotype|Conduction disorder of the heart
  • rs141124755Likely benignsingle nucleotide variantLong QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs145145511Likely benignsingle nucleotide variantCardiovascular phenotype|Long QT syndrome
  • rs149645600Likely benignsingle nucleotide variantCardiac arrest|Long QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs200628845Likely benignsingle nucleotide variantCardiovascular phenotype|Long QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs200765866Likely benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Cardiac arrhythmia, ankyrin-B-related
  • rs29388Likely benignsingle nucleotide variant
  • rs56256480Likely benignsingle nucleotide variant
  • rs750774547Likely benignsingle nucleotide variantLong QT syndrome|Cardiovascular phenotype|Hypertrophic cardiomyopathy
  • rs116253689Uncertain significancesingle nucleotide variantLong QT syndrome
  • rs142107156Uncertain significancesingle nucleotide variantLong QT syndrome
  • rs142534126Uncertain significancesingle nucleotide variantCardiovascular phenotype|Long QT syndrome|Cardiomyopathy
  • rs180843436Uncertain significancesingle nucleotide variantCongenital long QT syndrome|Catecholaminergic polymorphic ventricular tachycardia 1|Long QT syndrome
  • rs200124480Uncertain significancesingle nucleotide variantCardiovascular phenotype|Long QT syndrome
  • rs201071074Uncertain significancesingle nucleotide variantLong QT syndrome|Cardiac arrhythmia, ankyrin-B-related
  • rs202183785Uncertain significancesingle nucleotide variant
  • rs45608232Uncertain significancesingle nucleotide variantLong QT syndrome|Cardiovascular phenotype
  • rs752704424Uncertain 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.