Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE We conclude that the A allele of rs1447295 is associated with a higher risk of prostate cancer regardless of tumor aggressiveness, suggesting that such a variant, or a variant in linkage disequilibrium with it, plays a role early in prostate carcinogenesis. 17372260

2007

dbSNP: rs1447295
rs1447295
A 0.800 GeneticVariation GWASCAT Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. 17401363

2007

dbSNP: rs6983267
rs6983267
0.800 GeneticVariation BEFREE A combined analysis with four additional studies (total: 4,296 cases and 4,299 controls) confirms association with prostate cancer for rs6983267 in the centromeric locus (P = 9.42 x 10(-13); heterozygote odds ratio (OR): 1.26, 95% confidence interval (c.i.): 1.13-1.41; homozygote OR: 1.58, 95% c.i.: 1.40-1.78). 17401363

2007

dbSNP: rs6983267
rs6983267
G 0.800 GeneticVariation GWASCAT A combined analysis with four additional studies (total: 4,296 cases and 4,299 controls) confirms association with prostate cancer for rs6983267 in the centromeric locus (P = 9.42 x 10(-13); heterozygote odds ratio (OR): 1.26, 95% confidence interval (c.i.): 1.13-1.41; homozygote OR: 1.58, 95% c.i.: 1.40-1.78). 17401363

2007

dbSNP: rs1447295
rs1447295
A 0.800 GeneticVariation GWASCAT Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. 17401366

2007

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE These results further confirm the importance of these two polymorphic variants (rs1447295 and DG8S737) as risk factors for PC. 17409399

2007

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE The rs1447295 marker was strongly associated with prostate cancer among Caucasians (P = 1.23 x 10(-13)). 17409400

2007

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE Overall, there was a significant positive association between the A allele of the SNP rs1447295 and prostate cancer risk [odds ratio, 1.4; 95% confidence interval (95% CI), 1.1-2.0] but no significant association with the microsatellite DG8S737. 17416775

2007

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE We identified multiple SNPs in a 50-kb region (referred to as locus 1) that are in linkage disequilibrium with a previously reported risk-associated SNP at 8q24, rs1447295, but were more strongly associated with prostate cancer risk in our study population. 17925536

2007

dbSNP: rs6983267
rs6983267
0.800 GeneticVariation BEFREE Analysis of the National Cancer Institute's Cancer Genetic Markers of Susceptibility (CGEMS) prostate cancer association study database alone and in combination with our data provided further evidence for this second prostate cancer risk locus; in the combined analysis, the allele frequencies for rs6983267 differed statistically significantly between case patients and control subjects (P = 1.61 x 10(-9)). 17925536

2007

dbSNP: rs6983267
rs6983267
0.800 GeneticVariation BEFREE A meta-analysis across 10 studies including our results of four 8q24 variants (rs1442295 and DG8S737-region 1, rs16901979-region 2, and rs6983267-region 3) and prostate cancer risk demonstrated strong associations across a wide array of study designs and populations. 18231127

2008

dbSNP: rs6983267
rs6983267
G 0.800 GeneticVariation GWASCAT Multiple loci identified in a genome-wide association study of prostate cancer. 18264096

2008

dbSNP: rs6983267
rs6983267
G 0.800 GeneticVariation GWASCAT Multiple newly identified loci associated with prostate cancer susceptibility. 18264097

2008

dbSNP: rs6983267
rs6983267
0.800 GeneticVariation BEFREE We genotyped three variants associated with prostate cancer (rs10090154, rs13254738, and rs7000448), one associated with both prostate and colorectal cancer (rs6983267), and one associated with breast cancer (rs13281615) in a series of 1,499 breast cancer cases and 1,390 controls. 18349290

2008

dbSNP: rs7000448
rs7000448
0.030 GeneticVariation BEFREE We genotyped three variants associated with prostate cancer (rs10090154, rs13254738, and rs7000448), one associated with both prostate and colorectal cancer (rs6983267), and one associated with breast cancer (rs13281615) in a series of 1,499 breast cancer cases and 1,390 controls. 18349290

2008

dbSNP: rs13281615
rs13281615
0.020 GeneticVariation BEFREE We genotyped three variants associated with prostate cancer (rs10090154, rs13254738, and rs7000448), one associated with both prostate and colorectal cancer (rs6983267), and one associated with breast cancer (rs13281615) in a series of 1,499 breast cancer cases and 1,390 controls. 18349290

2008

dbSNP: rs6983267
rs6983267
0.800 GeneticVariation BEFREE Single nucleotide polymorphisms (SNPs) rs6983561 and rs6983267 showed the strongest evidence of prostate cancer association. 18360876

2008

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: rs13281615
rs13281615
0.020 GeneticVariation BEFREE Further studies are required to confirm whether the adjacent breast cancer-associated variant rs13281615 may be inversely associated with prostate cancer risk. 18625567

2009

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE The rs1447295 A allele was associated with susceptibility to PC (PC vs. non-PC: P = 0.041; OR, 1.28; 95%CI = 1.01-1.61), and was more significantly associated with disease in aggressive PC (aggressive PC vs. normal controls, P = 0.013; OR, 1.43; 95%CI = 1.08-1.90). 18726982

2008

dbSNP: rs6983267
rs6983267
0.800 GeneticVariation BEFREE The rs6983267 G allele did not show significant association with susceptibility to PC (PC vs. non-PC: P = 0.967; OR, 1.00; 95%CI = 0.83-1.21). 18726982

2008

dbSNP: rs7841264
rs7841264
0.010 GeneticVariation BEFREE However, the association between prostate cancer risk and the CC genotype of rs7841264, which marked the recombination hotspot at 8q24, was confined to patients with the highest Gleason score (odds ratio, 2.15; 95% confidence interval, 1.27-3.64; P=0.004). 18765558

2008

dbSNP: rs1447295
rs1447295
0.800 GeneticVariation BEFREE Overall, there was a positive association between carriers of the allele A of rs1447295 and prostate cancer risk [odds ratio (OR), 1.60; 95% confidence interval (95% CI), 1.01-2.52] but no significant association with carriers of alleles A of rs16901979 and allele G of rs6983267. 18768513

2008

dbSNP: rs6983267
rs6983267
0.800 GeneticVariation BEFREE There was no joint effect between SNPs rs16901979 A and rs6983267 G. These results confirm the significance of these SNPs in prostate cancer etiology in a previously unstudied population who do not undergo prostate cancer screening and are diagnosed with severe disease. 18768513

2008

dbSNP: rs6983267
rs6983267
0.800 GeneticVariation BEFREE One marker, rs6983267 on chromosome 8q24, has been linked to both colon and prostate cancer, and is therefore a good candidate for a multicancer susceptibility marker. 19047180

2008