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Gene entry

FANCC

FA complementation group C

Chromosome
9
Cytoband
9q22.32
Variants (rsID)
46

FANCC is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q22.32). Its official name is “FA complementation group C”. The reference table lists 46 variants (rsID) for this gene.

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Clinically classified variants

30 reference-table entries with clinical significance.

  • rs1800362Benignsingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group A|Fanconi anemia complementation group C|Malignant tumor of breast
  • rs201407189Benignsingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group C
  • rs55719336Benignsingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group C
  • rs138629441Conflicting interpretationssingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group C|Fanconi anemia complementation group A|Malignant tumor of breast
  • rs140781259Conflicting interpretationssingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group C|Fanconi anemia complementation group A|Malignant tumor of breast
  • rs141828876Conflicting interpretationssingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group C|Malignant tumor of breast
  • rs143181565Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Fanconi anemia complementation group C|Fanconi anemia complementation group A|Fanconi anemia|Malignant tumor of breast
  • rs1800361Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Fanconi anemia complementation group A|Fanconi anemia|Fanconi anemia complementation group C|Malignant tumor of breast
  • rs1800365Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Fanconi anemia complementation group C|Fanconi anemia complementation group A|Fanconi anemia|Malignant tumor of breast
  • rs1800366Conflicting interpretationssingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group C|Fanconi anemia complementation group A
  • rs368595927Conflicting interpretationssingle nucleotide variantFanconi anemia
  • rs375613884Conflicting interpretationssingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group C
  • rs41281202Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Fanconi anemia complementation group C|Fanconi anemia complementation group A|Fanconi anemia
  • rs587779902Conflicting interpretationssingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome
  • rs863224611Likely benignsingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome
  • rs370510954Likely pathogenicsingle nucleotide variantFanconi anemia complementation group C|Fanconi anemia|Hereditary cancer-predisposing syndrome
  • rs104886456Pathogenicsingle nucleotide variantFanconi anemia complementation group C|Fanconi anemia|Hereditary cancer-predisposing syndrome|Malignant tumor of breast
  • rs104886457Pathogenicsingle nucleotide variantFanconi anemia complementation group C|Fanconi anemia|Fanconi anemia complementation group C|Tracheoesophageal fistula|Hereditary cancer-predisposing syndrome
  • rs104886458Pathogenicsingle nucleotide variantFanconi anemia complementation group C|Fanconi anemia
  • rs104886459PathogenicDeletionFanconi anemia complementation group C|Fanconi anemia|Hereditary cancer-predisposing syndrome
  • rs1057516291Pathogenicsingle nucleotide variantFanconi anemia complementation group C|Fanconi anemia|Hereditary cancer-predisposing syndrome
  • rs121917783Pathogenicsingle nucleotide variantFanconi anemia complementation group C|Fanconi anemia|Hereditary cancer-predisposing syndrome|Malignant tumor of breast
  • rs121917784Pathogenicsingle nucleotide variantFanconi anemia complementation group C|Fanconi anemia|Hereditary cancer-predisposing syndrome
  • rs730881709PathogenicDuplicationFanconi anemia|Fanconi anemia complementation group C
  • rs730881731Pathogenicsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group C
  • rs769039987Pathogenicsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group C|Hereditary cancer-predisposing syndrome
  • rs774209201Pathogenicsingle nucleotide variantFanconi anemia complementation group C|Fanconi anemia|Hereditary cancer-predisposing syndrome
  • rs794726668Pathogenicsingle nucleotide variantFanconi anemia complementation group C|Fanconi anemia
  • rs863224441Pathogenicsingle nucleotide variantFanconi anemia
  • rs878853671PathogenicDuplicationFanconi 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.