Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2395655
rs2395655
Squamous cell carcinoma of esophagus
0.030 GeneticVariation BEFREE Subsequent specific RNA interference-mediated depletion or ectopic expression of LEDGF/p75 caused obviously down- or up-regulated expression of p21 mRNA in ESCC cells harboring rs2395655 GG genotype but not cells with rs2395655 AA genotype. 30854807

2019

dbSNP: rs2395655
rs2395655
Squamous cell carcinoma of esophagus
0.030 GeneticVariation BEFREE The rs3829963 C and rs2395655 G alleles, combined with cigarette smo</span>king, could further increase the risk for E</span>SCC (OR = 2.657 and OR = 2.828, respectively). 26932598

2016

dbSNP: rs2395655
rs2395655
Squamous cell carcinoma of esophagus
0.030 GeneticVariation BEFREE In the multiple genetic model, we found that the rs2395655 in CDKN1A is related with the risk of ESCC, and that the G allele increases the susceptibility to ESCC (OR: 1.364; 95% CI: 1.104-1.685). 24474449

2014

dbSNP: rs3176352
rs3176352
Squamous cell carcinoma of esophagus
0.010 GeneticVariation BEFREE p21 rs3176352 G>C and p73 rs1801173 C>T SNPs are associated with increased risk of ESCC. 24820515

2014

dbSNP: rs3829963
rs3829963
Squamous cell carcinoma of esophagus
0.010 GeneticVariation BEFREE The rs3829963 C and rs2395655 G alleles, combined with cigarette smoking, could further increase the risk for E</span>SCC (OR = 2.657 and OR = 2.828, respectively). 26932598

2016

dbSNP: rs762624
rs762624
Squamous cell carcinoma of esophagus
0.010 GeneticVariation BEFREE We found that the C allele of rs1009316 in Bax and rs762624 in CDKN1A can decrease the risk of ESCC. 24474449

2014