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Gene entry

FANCG

FA complementation group G

Chromosome
9
Cytoband
9p13.3
Variants (rsID)
8

FANCG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9p13.3). Its official name is “FA complementation group G”. The reference table lists 8 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs115131067Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group G
  • rs17885240Conflicting interpretationssingle nucleotide variantFanconi anemia|Inclusion Body Myopathy, Dominant|Amyotrophic Lateral Sclerosis, Dominant|Fanconi anemia complementation group G
  • rs121434426Pathogenicsingle nucleotide variantFanconi anemia complementation group G|Fanconi anemia
  • rs149616199Pathogenicsingle nucleotide variantFanconi anemia complementation group G|Fanconi anemia
  • rs200479612Pathogenicsingle nucleotide variantFanconi anemia complementation group G|Fanconi anemia
  • rs397507559Not classifiedDeletionFanconi anemia complementation group G

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.