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Gene entry

FANCD2

FA complementation group D2

Chromosome
3
Cytoband
3p25.3
Variants (rsID)
30

FANCD2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p25.3). Its official name is “FA complementation group D2”. The reference table lists 30 variants (rsID) for this gene.

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Clinically classified variants

15 reference-table entries with clinical significance.

  • rs147675860Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group D2
  • rs34557223Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group D2
  • rs34936017Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group D2
  • rs35495399Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group D2|Hereditary breast ovarian cancer syndrome
  • rs35782247Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group D2|Hereditary breast ovarian cancer syndrome
  • rs36070315Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A|Fanconi anemia complementation group D2|Hereditary breast ovarian cancer syndrome
  • rs36084488Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group D2|Hereditary breast ovarian cancer syndrome
  • rs55856815Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group D2
  • rs9811771Benignsingle nucleotide variantFanconi anemia complementation group D2|Fanconi anemia|Hereditary breast ovarian cancer syndrome
  • rs116736407Conflicting interpretationssingle nucleotide variantFanconi anemia
  • rs143936557Conflicting interpretationssingle nucleotide variantFanconi anemia
  • rs147426418Conflicting interpretationssingle nucleotide variantFanconi anemia complementation group D2|Fanconi anemia
  • rs17032279Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group D2|Hereditary breast ovarian cancer syndrome
  • rs201811817Pathogenicsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group D2
  • rs145099733Uncertain significancesingle nucleotide variantFanconi anemia complementation group D2|Fanconi anemia

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.