Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13181
rs13181
ERCC2 ; KLC3
0.040 GeneticVariation BEFREE The results demonstrated an association between the XPD Lys751Gln (rs13181) for frequency of presence C allele and risk for ESCC in the three ethnics of Yili Prefecture, in Xinjiang, China. 21553048

2012
dbSNP: rs13181
rs13181
ERCC2 ; KLC3
0.040 GeneticVariation BEFREE Polymorphic variation in COMT Val158Met and XPD Lys751Gln may be important for ESCC susceptibility. 20979431

2011
dbSNP: rs13181
rs13181
ERCC2 ; KLC3
0.040 GeneticVariation BEFREE To determine the effect of XPD genetic polymorphisms on the risk of esophageal squamous cell carcinoma (ESCC) and its interaction with carcinogen exposure, XPD polymorphisms at codon 312 (Asp-->Asn) and codon 751 (Lys-->Gln) were determined in 135 ESCC patients and 152 normal controls. 15381366

2004
dbSNP: rs13181
rs13181
ERCC2 ; KLC3
0.040 GeneticVariation BEFREE Neither Asp312Asn nor Lys751Gln polymorphisms in the XPD gene influenced risk of ESCC in our study. 12124811

2002