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Gene entry

FANCL

FA complementation group L

Chromosome
2
Cytoband
2p16.1
Variants (rsID)
18

FANCL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p16.1). Its official name is “FA complementation group L”. The reference table lists 18 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs11539575Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group L
  • rs139801716Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group L
  • rs149731356Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group L
  • rs848291Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group L
  • rs140088149Conflicting interpretationssingle nucleotide variantFanconi anemia
  • rs759217526Conflicting interpretationsDuplicationFanconi anemia|Fanconi anemia complementation group A|Fanconi anemia complementation group L

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.