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Gene entry

SLX4

SLX4 structure-specific endonuclease subunit

Chromosome
16
Cytoband
16p13.3
Variants (rsID)
27

SLX4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p13.3). Its official name is “SLX4 structure-specific endonuclease subunit”. The reference table lists 27 variants (rsID) for this gene.

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Clinically classified variants

18 reference-table entries with clinical significance.

  • rs113490934Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs114472821Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P|Malignant tumor of breast
  • rs115491049Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs143818824Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs149011965Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs28516461Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs376877866Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs3810812Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs3810813Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs7196345Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs75182789Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs79842542Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs141687678Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs143279888Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs146532299Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs150547487Conflicting interpretationssingle nucleotide variantFanconi anemia complementation group A|Fanconi anemia|Fanconi anemia complementation group P
  • rs181782315Uncertain significancesingle nucleotide variantFanconi anemia|Fanconi anemia complementation group P
  • rs200363140Uncertain significancesingle nucleotide variantFanconi 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.