Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7975232
rs7975232
VDR
0.030 GeneticVariation BEFREE SNP 4 had a significant protective effect (β=-0.6, p<0.05); whereas, SNP 7 (rs7975232) showed an increase association with prostate cancer risk and high Gleason score (β=0.32, p<0.05). 31243105

2019

dbSNP: rs731236
rs731236
VDR
0.030 GeneticVariation BEFREE Results Our findings suggest a significant association between rs731236 and prostate cancer risk in Asians and African Americans, but rs1544410 was not associated with prostate cancer under three genetic models. 28222630

2017

dbSNP: rs731236
rs731236
VDR
0.030 GeneticVariation BEFREE rs731236 and rs7975232 were significantly associated with PCa risk (p<0.05). 25750310

2015

dbSNP: rs7975232
rs7975232
VDR
0.030 GeneticVariation BEFREE rs731236 and rs7975232 were significantly associated with PCa risk (p<0.05). 25750310

2015

dbSNP: rs731236
rs731236
VDR
0.030 GeneticVariation BEFREE We also examined vitamin D related genes, VDR and CYP27B1, and found a significant association of PCa with the TaqI polymorphism (rs731236) in the former. 21358824

2011

dbSNP: rs7975232
rs7975232
VDR
0.030 GeneticVariation BEFREE Our findings suggest that the VDR ApaI (rs7975232) polymorphism may play a role in the development of sporadic PCa. 18849534

2008

dbSNP: rs1544410
rs1544410
VDR
0.020 GeneticVariation BEFREE The association between vitamin D receptor gene <i>Bsm I</i> (rs1544410) polymorphism and prostate cancer (PCa) risk has been investigated by numerous previous studies, which yielded inconsistent results. 30122987

2018

dbSNP: rs1544410
rs1544410
VDR
0.020 GeneticVariation BEFREE Results Our findings suggest a significant association between rs731236 and prostate cancer risk in Asians and African Americans, but rs1544410 was not associated with prostate cancer under three genetic models. 28222630

2017

dbSNP: rs2239182
rs2239182
VDR
0.010 GeneticVariation BEFREE The statistical analysis suggested that two VDR sequence variants (rs2408876 and rs2239182) had a significant association with prostate cancer risk (odds ratio [OR]. 24120391

2014

dbSNP: rs2408876
rs2408876
VDR
0.010 GeneticVariation BEFREE The statistical analysis suggested that two VDR sequence variants (rs2408876 and rs2239182) had a significant association with prostate cancer risk (odds ratio [OR]. 24120391

2014

dbSNP: rs11168314
rs11168314
VDR
0.010 GeneticVariation BEFREE Three VDR tagSNPs (rs3782905, rs7299460, and rs11168314), one CYP27B1 tagSNP (rs3782130), and five CYP24A1 tagSNPs (rs3787557, rs4809960, rs2296241, rs2585428, and rs6022999) significantly altered risks of PCa death. 20687218

2010

dbSNP: rs7299460
rs7299460
VDR
0.010 GeneticVariation BEFREE Three VDR tagSNPs (rs3782905, rs7299460, and rs11168314), one CYP27B1 tagSNP (rs3782130), and five CYP24A1 tagSNPs (rs3787557, rs4809960, rs2296241, rs2585428, and rs6022999) significantly altered risks of PCa death. 20687218

2010

dbSNP: rs11574143
rs11574143
VDR
0.010 GeneticVariation BEFREE Among men in the lowest tertile of serum 25(OH)D (<48.9 nmol/l), however, prostate cancer risk was related to tag SNPS in or near the 3' untranslated region (UTR) of VDR, with the strongest association for rs11574143 [odds ratio (95% confidence interval) for risk allele carriers versus wild-type: 2.49 (1.51-4.11), P = 0.0007]; the genotype associations were null among men in tertile 2 and tertile 3. 19255064

2009

dbSNP: rs2107301
rs2107301
VDR
0.010 GeneticVariation BEFREE In the genotype analysis, homozygotes at two VDR loci (rs2107301 and rs2238135) were associated with a 2- to 2.5-fold higher risk of prostate cancer compared with the homozygote common allele [odds ratio, 2.47 (95% confidence interval, 1.52-4.00; P = 0.002) and 1.95 (95% confidence interval, 1.17-3.26; P = 0.007), respectively; P value corrected for multiple comparisons for VDR = 0.002]. 17932346

2007

dbSNP: rs2238135
rs2238135
VDR
0.010 GeneticVariation BEFREE In the genotype analysis, homozygotes at two VDR loci (rs2107301 and rs2238135) were associated with a 2- to 2.5-fold higher risk of prostate cancer compared with the homozygote common allele [odds ratio, 2.47 (95% confidence interval, 1.52-4.00; P = 0.002) and 1.95 (95% confidence interval, 1.17-3.26; P = 0.007), respectively; P value corrected for multiple comparisons for VDR = 0.002]. 17932346

2007