Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs920778
rs920778
0.030 GeneticVariation BEFREE The association between the expression of rs920778 and BC, CC, and OC susceptibility was not clear (alleles T/C: OR = 1.28 [95% CI, 0.87-1.89]; in codominant model: CT/CC OR = 1.10, [95% CI, 0.71-1.71], TT/CC OR = 1.29 [95% CI, 0.59-2.80]; dominant model: TC + TT/CC OR = 1.16, [95% CI, 0.73-1.86]; and recessive model: TT/TC + CC OR = 1.43, [95% CI, 0.83-2.47]). 30484890

2018

dbSNP: rs920778
rs920778
0.030 GeneticVariation BEFREE We found a strong association between the SNP rs920778 in th</span>e intronic enhancer of the HOTAIR and cervical cancer (P<10-4). 27467165

2016

dbSNP: rs920778
rs920778
0.030 GeneticVariation BEFREE Moreover, the TT genotype of rs920778 might be a potent prognostic marker in cervical cancer patients. 27229487

2016

dbSNP: rs7958904
rs7958904
0.010 GeneticVariation BEFREE TCGA database showed the CC tis</span>sues with rs7958904</span> CC</span> genot</span>ype had higher HOTAIR expression than those with GG genotype (P = 0.046). 28600545

2017

dbSNP: rs1899663
rs1899663
0.010 GeneticVariation BEFREE We performed a case-control study including 510 cervical cancer patients (cases) and 713 cancer-free individuals (controls) to investigate the association between three haplotype-tagging SNPs (rs920778, rs1899663 and rs4759314) in the lncRNA HOTAIR and the risk of cervical cancer. 27467165

2016

dbSNP: rs4759314
rs4759314
0.010 GeneticVariation BEFREE We performed a case-control study including 510 cervical cancer patients (cases) and 713 cancer-free individuals (controls) to investigate the association between three haplotype-tagging SNPs (rs920778, rs1899663 and rs4759314) in the lncRNA HOTAIR and the risk of cervical cancer. 27467165

2016