Gene entry
XRCC2
X-ray repair cross complementing 2
- Chromosome
- 7
- Cytoband
- 7q36.1
- Variants (rsID)
- 7
XRCC2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q36.1). Its official name is “X-ray repair cross complementing 2”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs145085742Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Fanconi anemia complementation group U
- rs3218536Benignsingle nucleotide variantHereditary cancer-predisposing syndrome
- rs143153871Conflicting interpretationssingle nucleotide variantFanconi anemia complementation group U|Hereditary cancer-predisposing syndrome|Short stature, microcephaly, and endocrine dysfunction
- rs61762969Conflicting interpretationssingle nucleotide variantColon cancer|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group U
- rs180805457Uncertain significancesingle nucleotide variantHereditary cancer-predisposing syndrome
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.