Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799782
rs1799782
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.050 GeneticVariation BEFREE Taken together, there was no obvious association between the Arg194Trp or Arg280His polymorphism and cervical cancer risk. 27903984

2017

dbSNP: rs1799782
rs1799782
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.050 GeneticVariation BEFREE This meta-analysis provides strongly statistical evidence for the association between rs1799782 and cervical cancer risk, as well as its association with rs25487 only in Asian populations. 24057881

2014

dbSNP: rs1799782
rs1799782
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.050 GeneticVariation BEFREE The Arg194Trp polymorphism of XRCC1 increases risk of cervical cancer; the variant 399Gln allele predicts poor response to platinum-based chemotherapy, while the Arg194Trp polymorphism indicates a good response. 23464469

2012

dbSNP: rs1799782
rs1799782
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.050 GeneticVariation BEFREE This meta-analysis suggests that Arg194Trp polymorphism may be associated with CC risk, Arg399Gln polymorphism might be a low-penetrent risk factor for CC only in Asians, and there may be no association between Arg280His polymorphism and CC risk. 22984511

2012

dbSNP: rs1799782
rs1799782
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.050 GeneticVariation BEFREE The genotypes of XRCC1 Arginine194Tryptophan and GGH-401Cytosine/Thymine were associated with the response to NAC in patients with cervical cancer. 18851872

2008