Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs523349
rs523349
0.080 GeneticVariation BEFREE <i>SRD5A2</i> rs523349 (V89L) polymorphism showed no significant role in BPH occurrence in total analysis, but its reducing and increasing effects on the disease risk were reflected in Caucasian and other-ethnicity subgroups, respectively, after stratification analysis by ethnicity. 28955247

2017

dbSNP: rs523349
rs523349
0.080 GeneticVariation BEFREE For the V89L polymorphism there were no significant differences in genotype frequencies in patients with prostate cancer and controls (p = 0.071) or in patients with BPH and male controls (p = 0.219). 12771801

2003

dbSNP: rs523349
rs523349
0.080 GeneticVariation BEFREE The enzyme is a target in pharmacological treatment of benign prostatic hyperplasia using specific inhibitors such as finasteride.Makridakis et al. have characterized the V89L and A49T polymorphisms in recombinant expression systems. 12042668

2002

dbSNP: rs523349
rs523349
0.080 GeneticVariation BEFREE Although V89L was nonsignificantly associated with BPH in overall population, BPH risk increased significantly with the number of L alleles in Hispanics (P for trend=0.03). 16018939

2005

dbSNP: rs523349
rs523349
0.080 GeneticVariation BEFREE In men with a clinical diagnosis of benign prostatic hyperplasia (BPH), polytomous logistic regression analysis was conducted to evaluate associations between two silent polymorphisms in SRD5A1 (codon positions 30 and 116), two polymorphisms in SRD5A2 (Val89Leu substitution and C to T transition in intron 1), a trinucleotide (CAG)n repeat in androgen receptor (AR), and an Arg492Cys substitution in ADRA1A and clinical parameters that characterize severity of BPH. 15136785

2004

dbSNP: rs523349
rs523349
0.080 GeneticVariation BEFREE The SRD5A2 polymorphisms A49T, V89L and R227Q, the androgen receptor CAG and GGN repeats and sex hormone status was investigated in men with prostate cancer (CaP) (n=89), benign prostate hyperplasia (n=45) and healthy military conscripts (n=223). 16039774

2005

dbSNP: rs523349
rs523349
0.080 GeneticVariation BEFREE The aim of our study was to determine the frequency of the <i>SRD5A1</i> (rs6884552, rs3797177) and <i>SRD5A2</i> (rs523349, rs12470143) genes' polymorphisms, and to assess the relationships between the genotypes of the tested mutations, and the levels of biochemical and hormonal parameters in patients with BPH. 29084161

2017

dbSNP: rs523349
rs523349
0.080 GeneticVariation BEFREE CYP19 1531 C>T, SRD5A2 gene V89L, CYP17 gene -34 T/C, PSA-158 (G/A) regions were evaluated for the association between polymorphisms and benign prostatic hyperplasia and prostate cancer in study population. 26214411

2015

dbSNP: rs9282858
rs9282858
0.060 GeneticVariation BEFREE Prostate cancer and BPH were not associated with the alanine-49 to threonine single nucleotide polymorphism and the (TA)n repeat. 16018939

2005

dbSNP: rs9282858
rs9282858
0.060 GeneticVariation BEFREE The SRD5A2 polymorphisms A49T, V89L and R227Q, the androgen receptor CAG and GGN repeats and sex hormone status was investigated in men with prostate cancer (CaP) (n=89), benign prostate hyperplasia (n=45) and healthy military conscripts (n=223). 16039774

2005

dbSNP: rs9282858
rs9282858
0.060 GeneticVariation BEFREE The enzyme is a target in pharmacological treatment of benign prostatic hyperplasia using specific inhibitors such as finasteride.Makridakis et al. have characterized the V89L and A49T polymorphisms in recombinant expression systems. 12042668

2002

dbSNP: rs9282858
rs9282858
0.060 GeneticVariation BEFREE The A49T and TA repeat polymorphisms were not associated with BPH. 15389785

2005

dbSNP: rs9282858
rs9282858
0.060 GeneticVariation BEFREE We found statistically significant relationship between the SRD5A2 gene Ala49Thr (OR=2.3; CI 95%, 1.04-5.1; p=0.01<0.05) , but not the other polymorphisms, and B</span>PH. 21627373

2011

dbSNP: rs9282858
rs9282858
0.060 GeneticVariation BEFREE <b>Results:</b><i>SRD5A2</i> rs9282858 (A49T) polymorphism showed a significant correlation with increased B</span>PH susceptibility under allele T vs.allele A genetic model (OR = 2.51, 95% CI = 1.29-4.88) in total analysis, and stratification analysis by ethnicity also revealed a similar association in Caucasian group under the same contrast. 28955247

2017

dbSNP: rs149709822
rs149709822
0.020 GeneticVariation BEFREE The A49T and TA repeat polymorphisms were not associated with BPH. 15389785

2005

dbSNP: rs149709822
rs149709822
0.020 GeneticVariation BEFREE The enzyme is a target in pharmacological treatment of benign prostatic hyperplasia using specific inhibitors such as finasteride.Makridakis et al. have characterized the V89L and A49T polymorphisms in recombinant expression systems. 12042668

2002

dbSNP: rs1799864
rs1799864
0.020 GeneticVariation BEFREE In the present study, the aim was to evaluate the association of three polymorphisms in chemokine genes, namely C‑C motif chemokine ligand (CCL)2 rs1024611, CC chemokine receptor 2 (CCR2) rs1799864 and CCL5 rs2107538, with BPH risk. 30816510

2019

dbSNP: rs1799864
rs1799864
0.020 GeneticVariation BEFREE The impact of two chemokine receptor gene polymorphisms, CCR2-64I (rs1799864) and CCR5-Δ32 (rs333), was evaluated in BPH and PCa. 23632061

2013

dbSNP: rs1799983
rs1799983
0.020 GeneticVariation BEFREE The endothelial nitric oxide synthase Glu-298-Asp polymorphism and its mRNA expression in the peripheral blood of patients with prostate cancer and benign prostatic hyperplasia. 16458450

2006

dbSNP: rs1799983
rs1799983
0.020 GeneticVariation BEFREE The association of endothelial nitric oxide synthase (eNOS) G894T gene polymorphism with responsiveness to a selective α1 -blocker in men with benign prostatic hyperplasia related lower urinary tract symptoms. 26940040

2016

dbSNP: rs10035432
rs10035432
0.010 GeneticVariation BEFREE We found an inverse association between SNP rs10035432 and BPH under the log-additive (p=0.007) model. 26124326

2015

dbSNP: rs1024611
rs1024611
0.010 GeneticVariation BEFREE No association was observed between the CCL2 rs1024611 polymorphism and BPH. 30816510

2019

dbSNP: rs103294
rs103294
0.010 GeneticVariation BEFREE Association between rs103294, BPH risk and clinicopathological traits were tested with adjustment for age. rs103294 was significantly associated with BPH risk with a p-value of 0.0067. 23615473

2013

dbSNP: rs1034866440
rs1034866440
AR
0.010 GeneticVariation BEFREE The SRD5A2 polymorphisms A49T, V89L and R227Q, the androgen receptor CAG and GGN repeats and sex hormone status was investigated in men with prostate cancer (CaP) (n=89), benign prostate hyperplasia (n=45) and healthy military conscripts (n=223). 16039774

2005

dbSNP: rs1045531
rs1045531
0.010 GeneticVariation BEFREE Statistically significant differences in the distribution of the rs1045531 genotypes and alleles were found between prostate cancer and benign prostatic hyperplasia in patients undergoing prostate biopsy ( P = .035 and .046, respectively). 29332451

2017