Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs25487
rs25487
XRCC1
0.020 GeneticVariation BEFREE Moreover, the clearest differences were found for rs13181 in ERCC2 and rs25487 in XRCC1 between CLL patients with unfavorable cytogenetic aberrations and controls. 19484764

2009
dbSNP: rs25487
rs25487
XRCC1
0.020 GeneticVariation BEFREE The Arg399Gln polymorphism may be etiologically associated with CLL; however, it does not seem to increase SCE frequency. 22106831

2012