Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs25487
rs25487
XRCC1
0.030 GeneticVariation BEFREE Our results suggested that Arg399Gln variant of <i>XRCC1</i> gene might be a risk factor for NMSC in Asian populations, and Arg194Trp variant of <i>XRCC1</i> gene might be a protective factor for patients with SCC. 28761356

2017
dbSNP: rs25487
rs25487
XRCC1
0.030 GeneticVariation BEFREE In the current study, we aim to assess the impact of XRCC1 R399Q and XRCC3 T241M polymorphisms on the risk of NMSC associated with sunlight and arsenic exposure. 25218703

2014
dbSNP: rs25487
rs25487
XRCC1
0.030 GeneticVariation BEFREE The XRCC1 Arg399Gln polymorphism, sunburn, and non-melanoma skin cancer: evidence of gene-environment interaction. 11782372

2002