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Gene entry

TAP2

transporter 2, ATP binding cassette subfamily B member

Chromosome
6
Cytoband
6p21.32
Variants (rsID)
53

TAP2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p21.32). Its official name is “transporter 2, ATP binding cassette subfamily B member”. The reference table lists 53 variants (rsID) for this gene.

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Clinically classified variants

7 reference-table entries with clinical significance.

  • rs1042116Benignsingle nucleotide variantMHC class I deficiency
  • rs16870908Benignsingle nucleotide variant
  • rs1800454Benignsingle nucleotide variantPEPTIDE TRANSPORTER PSF2 POLYMORPHISM|MHC class I deficiency
  • rs2228397Benignsingle nucleotide variantMHC class I deficiency
  • rs241436Benignsingle nucleotide variantMHC class I deficiency
  • rs241442Benignsingle nucleotide variantMHC class I deficiency
  • rs241449Benignsingle nucleotide variantMHC class I deficiency

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.