Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE In particular, both homozygous AA and heterozygous CA genotypes of rs16901979, as well as the AA and CA genotypes of rs1447295, were associated with the risk of prostate cancer. 30061842

2018

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE There are strong association between rs1447295 polymorphism and prostate cancer susceptibility in different ethnic groups and different prostate cancer stage, suggesting that rs1447295 might serve as a reliable biomarker for prostate cancer diagnosis. 28978014

2017

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE Therefore, this meta-analysis demonstrated that 8q24 polymorphisms (rs6983267 T>G, rs1447295 C>A, rs16901979 C>A, rs6983561 A>C and rs10090154 C>T) were associated with the susceptibility to PCa, which held the potential biomarkers for PCa risk. 29158792

2017

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE The cumulative effects test of risk alleles (rs rs1983891, rs339331, rs16901966, rs1447295 and rs10090154) showed an increasing risk to PCa in a frequency-dependent manner (ptrend=0.001), and men with more than 3 risk alleles had the most significant susceptibility to PCa (OR=1.99, p=0.001), compared with those who had one risk allele (OR=1.17, p=0.486). 26537068

2016

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE Interestingly, the effect of rs1447295 on PCa risk was observed among Caucasians and Asians, but not Africa-Americans. 26159557

2015

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE The evidence for 8q24 SNPs with PCa risk in northern Chinese men showed rs16901966, rs1447295 and rs10090154 at 8q24 (region 1, region 2) to be strongly associated with PCa and clinical covariates. 24377597

2014

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE We showed statistically significant association of the A allele of rs1447295 (OR [CI 95%] = 1.96 [1.37-2.81], P<0.0001) and the T allele of rs10090154 (OR [CI 95%] = 2.14 [1.41-3.26], P<0.0001) with CaP. 23628314

2014

dbSNP: rs1447295
rs1447295
A 0.800 GeneticVariation GWASDB Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies. 24753544

2014

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation GWASDB Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population. 23555315

2013

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation GWASDB Evaluating genetic risk for prostate cancer among Japanese and Latinos. 22923026

2012

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE • The frequencies of three CaP risk alleles (rs1447295 [8q24], P= 0.004; rs1571801 [9q33.2], P= 0.03; rs11228565 [11q13], P= 0.02) were significantly higher in men with 'unfavourable' pathological characteristics. 22077888

2012

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE For northern Chinese men rs16901966, rs1447295, rs11986220 and rs10090154 at 8q24 (region 1, region 2) are associated with prostate cancer and prostate cancer related clinical covariates. 22099997

2012

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE The A allele at SNP rs1447295 was associated with the incidence of prostate cancer. 22583965

2012

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE Allele -8 of microsatellite DG8S737 with 22 repeats and allele A of the single-nucleotide polymorphism (SNP) rs1447295 have been found to be significantly associated with prostate cancer. 20700145

2011

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE There was a tendency towards significantly increased risk for SNPs rs1447295 and rs6983267 in men with early-onset prostate cancer. 21557270

2011

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE We demonstrate that trans-acting RNA molecules facilitating resistance to androgen depletion (RAD) in vitro and castration-resistant phenotype (CRP) in vivo of PC contain intergenic 8q24-locus SNP variants (rs1447295; rs16901979; rs6983267) that were recently linked with increased risk of PC. 22067658

2011

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE Correlation between genotypes and biopsy outcome (positive or negative) and Gleason score (≤6 or >6) were studied by univariate and multivariable analysis. rs1447295 and rs6983267 risk variants were found to be associated with the presence of PCa in univariate analysis. rs6983267 genotype remained significantly linked to a positive biopsy (odds ratio [OR] = 1.66, 95% confidence interval [CI]: 1.06-2.59, P = 0.026) in multivariable analysis, but rs1447295 genotype did not (OR = 1.47, 95% CI: 0.89-2.43, P = 0.13).When biopsy outcome was stratified according to Gleason score, risk variants of rs1447295 were associated with aggressive disease (Gleason score ≥7) in univariate and multivariable analysis (OR = 2.05 95% CI: 1.10-3.79, P = 0.023). rs6983267 GG genotype was not related to aggressiveness. 21308149

2011

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE Analysis of the cumulative risk of rs1447295, a confirmed risk variant, and one of these markers showed that compared to men who do not have any of these risk variants, men who carry any combination of 1 or 2 risk genotypes have a gradually increased prostate cancer risk (P for trend <0.001). 19908238

2010

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE In conclusion, the relationship between the rs1447295 and DG8S737 polymorphic variants on chromosome 8q24 and prostate cancer risk is seen in the Polish population to a similar degree as it has been observed elsewhere. 19952762

2010

dbSNP: rs1447295
rs1447295
A 0.800 GeneticVariation GWASDB Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. 19767754

2009

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE The A allele of rs1447295 was significantly associated with the risk of sporadic prostate cancer (p = 0.04; age-adjusted OR, 1.34), while the G allele of rs6983267 showed a trend towards being a high-risk allele (p = 0.06; age-adjusted OR, 1.27). 19602258

2009

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE Three prostate cancer susceptibility single-nucleotide polymorphisms (rs1447295 at 8q24, rs7920517 and rs10993994 at 10q11) were associated with prostate-specific antigen recurrence (P < 0.02). 19900942

2009

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE Our results corroborate previous reports of 8q24 as a prostate cancer susceptibility locus and provide evidence for rs1447295 as a potentially important genetic marker. 18625567

2009

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE This study confirmed that the A allele of rs1447295 is associated with a high risk of PCa in Taiwanese men. 19428064

2009

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE Forty-nine tagging SNPs including three previously reported significant variants (rs1447295, rs6983267, rs16901979) and seven variants in the 5' upstream region of the MYC proto-oncogene were tested for association with susceptibility to PC and tumor aggressiveness in 596 histologically verified PC cases and 567 ethnically matched controls. 19562729

2009