Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs773919809
rs773919809
0.030 GeneticVariation BEFREE Aberrant DNA methylation of P16, MGMT, and hMLH1 genes in combination with MTHFR C677T genetic polymorphism and folate intake in esophageal squamous cell carcinoma. 23244153

2012

dbSNP: rs773919809
rs773919809
0.030 GeneticVariation BEFREE No significant relation was observed between aberrant DNA methylation of P16, MGMT and hMLH1 gene, as well as MTHFR C677T genetic polymorphisms and the prognosis of ESCC. 21375764

2011

dbSNP: rs773919809
rs773919809
0.030 GeneticVariation BEFREE Aberrant DNA methylation of P16, MGMT, and hMLH1 genes in combination with MTHFR C677T genetic polymorphism in esophageal squamous cell carcinoma. 18199718

2008

dbSNP: rs7087131
rs7087131
0.010 GeneticVariation BEFREE The A allele of the rs7087131 variant of MGMT gene was associated with a decreased risk of ESCC under a dominant model (odds ratio, 0.79; 95% confidence interval, 0.64-0.96; P = 0.02). 19826048

2009