Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6959895
rs6959895 		T 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148

2017
dbSNP: rs6975391
rs6975391 		C 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148

2017
dbSNP: rs7148539
rs7148539 		C 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148

2017
dbSNP: rs765547
rs765547 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247

2016
dbSNP: rs7703051
rs7703051 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247

2016
dbSNP: rs799165
rs799165 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247

2016
dbSNP: rs8082812
rs8082812 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247

2016
dbSNP: rs8129326
rs8129326 		G 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148

2017
dbSNP: rs9323205
rs9323205 		G 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148

2017
dbSNP: rs9376307
rs9376307 		0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148

2017
dbSNP: rs9599474
rs9599474 		0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148

2017
dbSNP: rs971535
rs971535 		C 0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148

2017
dbSNP: rs9851042
rs9851042 		0.700 GeneticVariation GWASCAT Cancer risk susceptibility loci in a Swedish population. 29299148

2017
dbSNP: rs874945
rs874945 		0.050 GeneticVariation BEFREE However, there is no significant association between SNPs variants and cancer risk under any five genetic models for rs4759314, rs1899663 and rs874945. 30941992

2019
dbSNP: rs874945
rs874945 		0.050 GeneticVariation BEFREE The results showed that cancer risk was elevated in recessive mutation of rs12826786 (TT vs CC+CT: OR =1.55, 95% CI =1.19, 2.03; TT+CT vs CC: OR =1.23, 95% CI =1.04, 1.46; TT vs CC: OR =1.67, 95% CI =1.24, 2.24; T vs C: OR =1.24, 95% CI =1.09, 1.40) and rs920778 (TT vs CC+CT: OR =1.73, 95% CI =1.30, 2.30; TT+CT vs CC: OR =1.40, 95% CI =1.16, 1.70; TT vs CC: OR =1.83, 95% CI =1.25, 2.68; T vs C: OR =1.37, 95% CI =1.18, 1.59), while the results for polymorphisms of rs7958904, rs4759314, rs874945, and rs1899663 were insignificant. 29497311

2018
dbSNP: rs874945
rs874945 		0.050 GeneticVariation BEFREE HOTAIR SNP rs920778, rs7958904 and rs8749</span>45 are susceptible to cancer risk. 27965458

2017
dbSNP: rs874945
rs874945 		0.050 GeneticVariation BEFREE However, no significant association was found between the rs1899663, rs874945, and rs4759314 polymorphisms and susceptibility of cancer. 29463216

2018
dbSNP: rs874945
rs874945 		0.050 GeneticVariation BEFREE However, no significant association was identified between the rs874945, rs4759314 and rs1899663 polymorphisms and cancer susceptibility. 27791260

2017
dbSNP: rs12826786
rs12826786 		0.030 GeneticVariation BEFREE Our meta-analysis showed that HOTAIR polymorphisms of rs12826786 and rs920778 were correlated with increased cancer risk, while rs7958904, rs4759314, rs874945, and rs1899663 were not. 29497311

2018
dbSNP: rs12826786
rs12826786 		0.030 GeneticVariation BEFREE The HOTAIR single nucleotide polymorphisms (SNPs) rs920778 (C > T) and rs12826786 (C > T) present in the intronic enhancer and promoter regions of HOTAIR, respectively, are associated with expression, cancer susceptibility, and patient prognosis in some tumor types. 28083786

2017
dbSNP: rs12826786
rs12826786 		0.030 GeneticVariation BEFREE For the rs12826786 polymorphism, we identified it significantly increased susceptibility to cancer risk in all genetic models rather than heterozygous models. 29463216

2018
dbSNP: rs2046210
rs2046210 		0.020 GeneticVariation BEFREE With the exception of rs2046210 at 6q25.1, the seven other SNPs showed a stronger association with ER-positive than ER-negative cancer. 23535825

2013
dbSNP: rs2046210
rs2046210 		0.020 GeneticVariation BEFREE In The Cancer Genome Atlas samples, the AA/AG risk genotypes of SNP rs2046210 were associated with a significantly higher expression level of the AKAP12 gene and a lower level of the ESR1 gene in tumor tissue. 26645718

2016
dbSNP: rs2069514
rs2069514 		0.020 GeneticVariation BEFREE The results showed that no significant associations with the risk of cancer were found in any model (allele contrast, codominant, dominant, or recessive model) in terms of rs2069514 and rs3569413 when all studies were pooled into a meta-analysis. 23462460

2013
dbSNP: rs2069514
rs2069514 		0.020 GeneticVariation BEFREE The previously published data on the association between CYP1A2*1C (rs2069514) and CYP1A2*1F (rs762551) polymorphisms and cancer risk have remained controversial. 25472037

2015