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Gene entry

ABCC2

ATP binding cassette subfamily C member 2

Chromosome
10
Cytoband
10q24.2
Variants (rsID)
82

ABCC2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q24.2). Its official name is “ATP binding cassette subfamily C member 2”. The reference table lists 82 variants (rsID) for this gene.

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Clinically classified variants

41 reference-table entries with clinical significance.

  • rs113646094Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs1137968Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs17216198Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs17216275Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs17216317Benignsingle nucleotide variant
  • rs17222561Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs17222596Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs17222617Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs17222723Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs2273697Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs3740066Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs7080681Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs7899457Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs8187692Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs8187707Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs8187709Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs8187710Benignsingle nucleotide variantDubin-Johnson syndrome
  • rs927344Benignmissense_variantDubin-Johnson Syndrome
  • rs17222540Conflicting interpretationssingle nucleotide variantDubin-Johnson syndrome
  • rs17222589Conflicting interpretationssingle nucleotide variantDubin-Johnson syndrome
  • rs17222624Conflicting interpretationssingle nucleotide variantDubin-Johnson syndrome
  • rs17222674Conflicting interpretationssingle nucleotide variantDubin-Johnson syndrome
  • rs45441199Conflicting interpretationssingle nucleotide variantDubin-Johnson syndrome
  • rs56131651Conflicting interpretationssingle nucleotide variantDubin-Johnson syndrome
  • rs112758556Likely benignsingle nucleotide variantDubin-Johnson syndrome
  • rs17222554Likely benignsingle nucleotide variantDubin-Johnson syndrome
  • rs146405172Likely pathogenicsingle nucleotide variantPseudoxanthoma elasticum
  • rs17222547Pathogenicsingle nucleotide variant
  • rs183923599Pathogenicsingle nucleotide variant
  • rs34937870Pathogenicsingle nucleotide variantDubin-Johnson syndrome
  • rs72558199Pathogenicsingle nucleotide variantDubin-Johnson syndrome
  • rs72558200Pathogenicsingle nucleotide variantDubin-Johnson syndrome
  • rs138221862Uncertain significancesingle nucleotide variantDubin-Johnson syndrome
  • rs145520251Uncertain significancesingle nucleotide variant
  • rs145672804Uncertain significancesingle nucleotide variantDubin-Johnson syndrome
  • rs148835620Uncertain significancesingle nucleotide variant
  • rs149200446Uncertain significancesingle nucleotide variant
  • rs17216324Uncertain significancesingle nucleotide variant
  • rs17222744Uncertain significancesingle nucleotide variantDubin-Johnson syndrome
  • rs201658889Uncertain significancesingle nucleotide variant
  • rs4267009Uncertain significancesingle nucleotide variantDubin-Johnson 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.