Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7516
Gene Symbol: XRCC2
XRCC2
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		0.540 GermlineCausalMutation ORPHANET Thus, XRCC2 acts late in the FA-BRCA pathway as also suggested by hypersensitivity of 900677A cells to ionising radiation. 27208205

2016
Entrez Id: 7516
Gene Symbol: XRCC2
XRCC2
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		0.540 GermlineCausalMutation ORPHANET Conclusion This study implicates XRCC2 in the pathogenesis of FA and calls for further investigation of the potential contribution of XRCC2 mutations to the overall mutational load of FA. 22232082

2012