Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17632542
rs17632542
0.750 GeneticVariation BEFREE Previous research identified four single nucleotide polymorphisms (SNPs) principally associated with circulating PSA levels rather than with prostate cancer risk (TERT rs2736098, FGFR2 rs10788160, TBX3 rs11067228, KLK3 rs17632542). 26431041

2015

dbSNP: rs17632542
rs17632542
T 0.750 GeneticVariation GWASDB When comparing prostate cancer cases with low PSA controls, alleles at genetic markers rs1512268, rs445114, rs10788160, rs11199874, rs17632542, rs266849, and rs2735839 were associated with an increased risk of prostate cancer, but the effect-estimates were attenuated to the null when using high PSA controls (Pheterogeneity in effect-estimates < 0.04). 24753544

2014

dbSNP: rs17632542
rs17632542
0.750 GeneticVariation BEFREE The genotypes of 4 single nucleotide polymorphisms previously associated with serum prostate specific antigen levels (rs2736098, rs10788160, rs11067228 and rs17632542) were determined in 964 healthy Caucasian volunteers without prostate cancer. 23246478

2013

dbSNP: rs17632542
rs17632542
0.750 GeneticVariation BEFREE The second locus was rs1354774 (P = 1.25 x 10(-12)), near KLK2 at 19q13, which was not associated with tPSA levels, and is separate from the rs17632542 locus at KLK3 that was previously associated with tPSA levels and prostate cancer risk. 23359319

2013

dbSNP: rs17632542
rs17632542
0.750 GeneticVariation BEFREE We did not observe a strong association with the KLK3 variant, reported in previous studies to confer risk for prostate cancer (rs2735839; P = 0.20) but did observe three highly correlated SNPs (rs17632542, rs62113212 and rs62113214) associated with prostate cancer [P = 3.41 × 10(-4), per-allele trend odds ratio (OR) = 0.77, 95% CI = 0.67-0.89]. 21318478

2011

dbSNP: rs17632542
rs17632542
0.750 GeneticVariation BEFREE We propose that rs17632542 may directly influence PrCa risk. 21465221

2011

dbSNP: rs1058205
rs1058205
0.720 GeneticVariation BEFREE The overall results indicated that polymorphism T>C of rs1058</span>205 was associated with decreased risk of PCa</span> (allele contrast: OR = 0.75, 95% CI = 0.64-0.88, <i>P</i><sub>heterogeneity</sub> < 0.001; homozygote comparison: OR = 0.58, 95% CI = 0.42-0.81, <i>P</i><sub>heterogeneity</sub> < 0.001), particularly in Caucasian population (allele contrast: OR = 0.77, 95% CI = 0.65-0.91, <i>P</i><sub>heterogeneity</sub> < 0.001; homozygote comparison: OR = 0.58, 95% CI = 0.41-0.82, <i>P</i><sub>heterogeneity</sub> < 0.001). 30413614

2018

dbSNP: rs1058205
rs1058205
0.720 GeneticVariation BEFREE The frequency of the TC genotype of rs1058205 in the PCa group was significantly lower than that in the control group (P = 0.049). 28272245

2017

dbSNP: rs1058205
rs1058205
0.720 GeneticVariation GWASDB Multiple newly identified loci associated with prostate cancer susceptibility. 18264097

2008

dbSNP: rs266882
rs266882
0.050 GeneticVariation BEFREE In addition, no association was observed between polymorphism A>G of rs266882 and risk of PCa. 30413614

2018

dbSNP: rs266882
rs266882
0.050 GeneticVariation BEFREE We evaluated the impact of genetic variation in the prostate-specific antigen (PSA) gene (rs266882) on serum PSA levels in healthy men as well as risk factors for benign prostate hypertrophy (BPH) and prostate cancer. 23315126

2013

dbSNP: rs266882
rs266882
0.050 GeneticVariation BEFREE Association of G/A polymorphism, rs266882, in AREI region of the prostate-specific antigen gene with prostate cancer risk and clinicopathological features. 23235975

2012

dbSNP: rs266882
rs266882
0.050 GeneticVariation BEFREE Meta-analysis of 12 studies of rs266882 and overall p</span>rostate cancer risk was null. 18827812

2008

dbSNP: rs266882
rs266882
0.050 GeneticVariation BEFREE Men homozygous or heterozygous for the G/G (rs925013/rs266882) haplotype were at higher risk of prostate cancer than men homozygous for the A/A haplotype (odds ratio, 1.3; 95% CI, 1.1-1.7; P = 0.009). 16775173

2006

dbSNP: rs149709822
rs149709822
0.040 GeneticVariation BEFREE This study tested the interactions of VDR (CDX2, FokI) and SRD5A2 (V89L, A49T) polymorphisms, and their associations with prostate cancer. 18483391

2008

dbSNP: rs149709822
rs149709822
0.040 GeneticVariation BEFREE Cytosine-adenine-guanine repeat length of the androgen receptor gene and the A49T and V89L polymorphisms of the 5 alpha-reductase (SRD5A2) gene have been associated with prostate cancer. 12210487

2002

dbSNP: rs149709822
rs149709822
0.040 GeneticVariation BEFREE The SRD5A2 V89L and A49T polymorphisms were, however, not associated with altered prostate cancer risk. 12042668

2002

dbSNP: rs149709822
rs149709822
0.040 GeneticVariation BEFREE Our results suggest that the A49T mutation may influence the pathological characteristics of prostate cancers and, thus, may affect the prognosis of these patients. 10749132

2000

dbSNP: rs61752561
rs61752561
0.020 GeneticVariation BEFREE The rs61752561 SNP appears to have a potential role in PCa pathogenesis by changing the glycosylation, protein stability, and PSA activity and may also affect the clinically measured F/T PSA ratio. 30538125

2019

dbSNP: rs61752561
rs61752561
0.020 GeneticVariation BEFREE The rs61752561 in KLK3 and rs2735839 in the KLK2-KLK3 intergenic region were strongly associated with prostate cancer-specific survival, and rs10486567 in the 7JAZF1 gene were associated with biochemical recurrence. 20460480

2010

dbSNP: rs746367915
rs746367915
0.020 GeneticVariation BEFREE An association of a single nucleotide polymorphism (SNP) of the KLK2 gene (rs198977; c.748C>T; R250W) with risk for developing prostate cancer has been observed. 21178268

2010

dbSNP: rs746367915
rs746367915
0.020 GeneticVariation BEFREE This exploratory analysis in prostate cancer patients revealed the W allele of the KLK2 R250W SNP to be less likely associated with low GS morphology. 21178268

2010

dbSNP: rs746367915
rs746367915
0.020 GeneticVariation BEFREE Our results suggest that the C allele of the functional C748T polymorphism of KLK2 may increase the risk of PCa. 15643194

2005

dbSNP: rs1192131078
rs1192131078
0.010 GeneticVariation BEFREE Recently, the rs61752561 SNP (Asp84Asn substitution) in exon 3 of the kallikrein-related peptidase 3 (<i>KLK3</i>) gene encoding prostate-specific antigen (PSA) was reported to be strongly associated with PCa risk (<i>P</i> = 2.3 × 10<sup>-8</sup>). 30538125

2019

dbSNP: rs369223448
rs369223448
0.010 GeneticVariation BEFREE Furthermore, XB130 knockdown hindered transition of G1 to S phase in prostate cancer cell line DU145 and LNCap, which might contribute to the inhibition of cellular proliferation. 27509056

2016