Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11549465
rs11549465
0.050 GeneticVariation BEFREE Our findings indicate that HIF1A rs11549465 polymorphism may not independently play a significant role in the occurrence of prostate cancer. 28415653

2017

dbSNP: rs11549465
rs11549465
0.050 GeneticVariation BEFREE The HIF1A +1772 C>T (rs11549465) polymorphism was genotyped, using DNA isolated from peripheral blood, in 1490 male subjects (754 with prostate cancer and 736 controls cancer-free) through Real-Time PCR. 24090974

2014

dbSNP: rs11549465
rs11549465
0.050 GeneticVariation BEFREE The current findings suggest that HIF1A P582S polymorphism correlates with urinary cancers risk in Caucasian population, while A588T polymorphism may increase the risk of urinary cancers in Asian population and prostate cancer. 23723982

2013

dbSNP: rs11549465
rs11549465
0.050 GeneticVariation BEFREE No altered PCa risk was associated with the rs11549465 and rs2057482 polymorphism. 23042446

2012

dbSNP: rs11549465
rs11549465
0.050 GeneticVariation BEFREE Our data suggest that homozygous HIF1A P582S mutation confers significant susceptibility to prostate cancer. 16998808

2007

dbSNP: rs11549467
rs11549467
0.030 GeneticVariation BEFREE The current findings suggest that HIF1A P582S polymorphism correlates with urinary cancers risk in Caucasian population, while A588T polymorphism may increase the risk of urinary cancers in Asian population and prostate cancer. 23723982

2013

dbSNP: rs11549467
rs11549467
0.030 GeneticVariation BEFREE However, the combined variant genotypes of rs2057482 and rs11549467 were associated with increased PCa risk (OR=2.10; 95%CI=1.23-3.57 among subjects carrying three or more risk alleles). 23042446

2012

dbSNP: rs11549467
rs11549467
0.030 GeneticVariation BEFREE No significant differences were found between the frequencies of A588T mutation in prostate cancer patients and controls. 16998808

2007

dbSNP: rs2057482
rs2057482
0.010 GeneticVariation BEFREE However, the combined variant genotypes of rs2057482 and rs11549467 were associated with increased PCa risk (OR=2.10; 95%CI=1.23-3.57 among subjects carrying three or more risk alleles). 23042446

2012