Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1859962
rs1859962
0.770 GeneticVariation BEFREE For rs1859962 at 17q24, genotype dependent expression was observed for the candidate target gene SOX9 in TMPRSS2:ERG fusion-positive PrCa, which was not evident in TMPRSS2:ERG negative tumors. 27798103

2016

dbSNP: rs1859962
rs1859962
0.770 GeneticVariation BEFREE We observed no association of the SNPs and the risk of developing PCa (OR 0.84, 95 % CI 0.30-2.38, p = 1.0 to rs1859962 and OR 1.94, 95 % CI 0.57-6.52, p = 0.28 to rs4430796), both sporadic and hereditary. 24627192

2014

dbSNP: rs1859962
rs1859962
0.770 GeneticVariation BEFREE Genotype TG on 11q13 (rs7931342, T) could be related to an increased Gleason score, AG on HNF1B (rs4430796, A) could be associated with PSA increase, and TG on 17q24 (rs1859962, G) could be negatively associated with an increased BMI in Chinese men with PCa. 23464444

2012

dbSNP: rs1859962
rs1859962
0.770 GeneticVariation BEFREE This identifies a PCa-specific enhancer within the rs1859962 risk LD block that establishes a 1-Mb chromatin loop with the SOX9 gene. 22665440

2012

dbSNP: rs1859962
rs1859962
0.770 GeneticVariation BEFREE Our results show that polymorphism of the G allele of SNP rs1859962 is associated with the risk of prostate cancer in a Chinese population. 21959049

2011

dbSNP: rs1859962
rs1859962
0.770 GeneticVariation BEFREE Furthermore, the SNPs rs6983561 and rs4430796 were associated with a susceptibility to aggressive prostate cancer, whereas rs1859962 was associated with non-aggressive prostate cancer. 21557267

2011

dbSNP: rs1859962
rs1859962
G 0.770 GeneticVariation GWASDB Genome-wide association study identifies new prostate cancer susceptibility loci. 21743057

2011

dbSNP: rs1859962
rs1859962
T 0.770 GeneticVariation GWASDB Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. 19767753

2009

dbSNP: rs1859962
rs1859962
0.770 GeneticVariation BEFREE Recent studies have identified 2 distinct genetic variants along chromosome 17, including allele T of single nucleotide polymorphism rs4430796 on 17q12 and allele G of single nucleotide polymorphism rs1859962 on 17q24, that have been linked to prostate cancer risk. 19371897

2009

dbSNP: rs1859962
rs1859962
G 0.770 GeneticVariation GWASDB Multiple newly identified loci associated with prostate cancer susceptibility. 18264097

2008