rs523349, SRD5A2

N. diseases: 21
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 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
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE Furthermore, SRD5A2 rs523349 polymorphism may be a promising biomarker for metastatic prostate cancer patients treated with primary ADT and a molecular target for advanced prostate cancer. 26169017 2015
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE It was confirmed that in the population studied, the SRD5A2 V89L polymorphism was not associated with the risk of prostate cancer and SRD5A2 was not shown to be a key gene involved in prostate cancer development. 25310105 2014
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE Although there was no overall association between V89L and prostate cancer risk, A49T might play a role in the etiology of prostate cancer among Caucasians. 23277398 2013
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE However, no clear consensus has been reached on the association between the SRD5A2 V89L, A49T and TA repeat polymorphisms and prostate cancer (PCa) risk. 21177315 2011
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE The authors found that prostate cancer was not associated with V89L (L allele vs. V allele: odds ratio = 0.99, 95% confidence interval: 0.94, 1.05) and was probably not associated with A49T (T allele vs. A allele: odds ratio = 1.10, 95% confidence interval: 0.86, 1.40). 19914946 2010
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE Our study suggests SRD5A2 V89L polymorphism could play a low-penetrant role in PCa risk among Europeans and individuals younger than 65 years. 19760631 2010
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE We evaluated the relationship of two single-nucleotide polymorphisms, A49T and V89L, with prostate cancer risk in a case-control study. 19215786 2009
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE Our results indicate that the SRD5A2 V89L VV genotype interacts with VDR FokI TT/CT genotypes in NHW men and VDR CDX2 GG genotypes in HW men to increase the risk for prostate cancer. 18483391 2008
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE Thirty-three men with early onset prostate cancer (PCa) were genotyped for the SRD5A2 V89L substitution and other polymorphisms in genes encoding receptors or enzymes that play important roles in pathways of steroid metabolism to ascertain if they were associated with standard clinical measures of disease progression at the time of diagnosis. 18780294 2008
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE However, the absence of an overall association between V89L genotype and aggressive prostate cancer argues for a cautious interpretation of these observations. 18268111 2008
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE In Caucasians, the HSD3B2 (TG)n,(TA)n,(CA)n intron 3 length polymorphism is associated with both prostate cancer risk and aggressiveness and the SRD5A2 V89L polymorphism may modify the risk conferred by this polymorphism. 17823934 2007
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE Controversy exists over the significance of associations between the SRD5A2 (5alpha-reductase type 2) polymorphisms, A49T and V89L, and risk of prostate cancer. 17136762 2007
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE Our data confirm in a large and homogeneous Caucasian French population that the low-activity V89L variant is associated with an increased risk of aggressive prostate cancer. 17448593 2007
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE These observations have suggested that the CYP17 A2/A2, CYP1B1 Val/Val, and CYP2D6 genotypes may be associated with an altered risk of prostate cancer, while the CYP2D6 and SRD5A2 V89L polymorphism have no association with its risk in the North Indian population. 16716118 2006
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 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
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE Overall, the V89L variant was associated with prostate cancer; the OR for men with the leucine-leucine (LL) genotype compared to men with the valine-valine (VV) genotype was 4.47 (95% CI, 1.24-16.18). 16018939 2005
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE These findings suggest that the SRD5A2 V89L variant may influence risk of developing prostate cancer, especially among men with a younger age of diagnosis or more aggressive disease. 14991867 2004
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE The V allele of the V89L polymorphism in the SRD5A2 gene may dominantly increase the risk of prostate cancer. 12771801 2003
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE We exclude a role for the V89L polymorphism in conferring susceptibility to prostate cancer. 12869400 2003
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE Our results do not support the hypothesis that the V89L and A49T polymorphisms in the SRD5A2 gene are related to the risk of prostate cancer, but are compatible with the suggestion from earlier studies that men who are homozygous for the TA(9) or (18) alleles and men who have the TA(9)/TA(18) genotype are at a modestly reduced risk. 12712437 2003
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE Three SNPs in the SRD5A2 gene (A49T, V89L, and C682G) and two microsatellite markers near SRD5A2 were genotyped in 159 HPC families to assess their linkage to prostate cancer. 12746845 2003
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 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
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE The aim of the present study was to evaluate the distribution of polymorphisms for the androgen receptor (AR) (CAG, StuI, GGN), SRD5A2 (Ala49Thr, Val89Leu) and CYP17 (MspA1) genes that are considered to be relevant for risk of prostate cancer. 11847524 2002
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.100 GeneticVariation BEFREE Further studies of the V89L polymorphism may lead to better understanding of the etiology of pros</span>tate cancer metastases. 12042668 2002