Gene: XPC ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2228000
rs2228000
XPC
0.020 GeneticVariation BEFREE XPC rs1870134-rs2228000-rs2228001-rs2470352-rs2607775 GCAAG haplotype conferred increased risk of GC compared with AG (OR=1.88, P= 6.98 × 10-4). 26760766

2016
dbSNP: rs2228000
rs2228000
XPC
0.020 GeneticVariation BEFREE With respect to Ala499Val and PAT-/+polymorphisms, we also did not observe any significant association with gastric cancer risk in the pooled analysis. 24886180

2014
dbSNP: rs1870134
rs1870134
XPC ; LSM3
0.010 GeneticVariation BEFREE XPC rs1870134-rs2228000-rs2228001-rs2470352-rs2607775 GCAAG haplotype conferred increased risk of GC compared with AG (OR=1.88, P= 6.98 × 10-4). 26760766

2016
dbSNP: rs2470352
rs2470352
XPC
0.010 GeneticVariation BEFREE XPC rs1870134-rs2228000-rs2228001-rs2470352-rs2607775 GCAAG haplotype conferred increased risk of GC compared with AG (OR=1.88, P= 6.98 × 10-4). 26760766

2016
dbSNP: rs2607775
rs2607775
XPC ; LSM3
0.010 GeneticVariation BEFREE XPC rs1870134-rs2228000-rs2228001-rs2470352-rs2607775 GCAAG haplotype conferred increased risk of GC compared with AG (OR=1.88, P= 6.98 × 10-4). 26760766

2016
dbSNP: rs535242729
rs535242729
XPC
0.010 GeneticVariation BEFREE Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), nucleotide excision repair (XPC-PAT, XPA-23G>A, ERCC1-19007T>C and XPD-L751Q), recombination (XRCC3-T241M) and alkylation damage reversal (MGMT-L84F) were tested for their potential role in the development of GC by using logistic regression models. 20817763

2010