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Gene entry

FANCF

FA complementation group F

Chromosome
11
Cytoband
11p14.3
Variants (rsID)
11

FANCF is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p14.3). Its official name is “FA complementation group F”. The reference table lists 11 variants (rsID) for this gene.

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Clinically classified variants

9 reference-table entries with clinical significance.

  • rs10500938Benignsingle nucleotide variantFanconi anemia complementation group F
  • rs113910234Benignsingle nucleotide variantFanconi anemia complementation group F|Fanconi anemia|Malignant tumor of breast
  • rs146647469Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group F
  • rs36045913Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group F
  • rs45451294Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group F
  • rs45556032Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group F
  • rs201215734Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group F
  • rs372625322Conflicting interpretationssingle nucleotide variantFanconi anemia
  • rs730880277PathogenicDeletionFanconi anemia complementation group F|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.