rs2228000, XPC

N. diseases: 53
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
0.050 GeneticVariation BEFREE We found that a significantly decreased risk of colorectal cancer was associated with XPC polymorphism rs2228000_CT genotype (OR 0.59; p < 0.0001) and the rs2228000_TT genotype (OR 0.29; p < 0.0001) compared to the reference genotype (CC). 25391773 2015
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
0.050 GeneticVariation BEFREE The relationships between XPC polymorphisms (Lys939Gln and Ala499Val) and the susceptibility to colorectal cancer (CRC) have been studied by several researchers, but the results were inconclusive. 26214629 2015
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
0.050 GeneticVariation BEFREE Individuals with variant genotypes of XPC Ala499Val appeared to be associated with the increased risk of CRC. 25355595 2015
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
0.050 GeneticVariation BEFREE This meta-analysis suggested that both the XPC Lys939Gln and Ala499Val polymorphisms were not risk factors for increasing colorectal cancer. 24385304 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
0.050 GeneticVariation BEFREE Though no significant association between Ala499Val and CRC risk was observed, we found that individuals carrying the CT+TT genotypes showed a significantly decreased risk of rectal cancer (OR=0.7; 95% CI=0.5-1.0). 21104992 2011