Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Strong significant associations were found between rs4430796 A and the risk of both prostate cancer (OR = 1.247, p = 2.21 × 10<sup>- 77</sup>) and endometrial cancer (OR = 1.217, p = 8.98 × 10<sup>- 16</sup>); the AA, AG genotypes also showed strong significant associations with the risk of prostate cancer (OR1 = 1.517, p = 4.46 × 10<sup>- 22</sup>; OR2 = 1.180, p = 0.002). 30053805

2018

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Our results suggested that the HNF1B rs4430796 (A>G) polymorphism decreased the risk of prostate cancer. 26214421

2015

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE The polymorphism rs4430796 of the chromosome 17q12 appears to be a biomarker for cancer aggressiveness, increased PSA and tumor volume of PCa. 24627192

2014

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE After subgroup analyses stratified by ethnicity, however, the rs4430796 polymorphism was significantly associated with prostate cancer in both Caucasians and Asians but not in African-Americans. 25177939

2014

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Individuals with the rs4430796 TT genotype were at increased CaP risk in the Chinese via a recessive model (odds ratios (OR) = 1.56, 95% CI = 1.04-2.33). 22561070

2013

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Six markers associated with early-onset prostate cancer [rs2171492 (7q32), rs6983561 (8q24), rs10993994 (10q11), rs4430796 (17q12), rs1799950 (17q21), and rs266849 (19q13)] were genotyped. 22144497

2012

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Genotype TG on 11q13 (rs7931342, T) could be related to an increased Gleason score, AG on HNF1B (rs4430796, A) could be associated with PSA increase, and TG on 17q24 (rs1859962, G) could be negatively associated with an increased BMI in Chinese men with PCa. 23464444

2012

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Ten SNPs were significantly related to prostate cancer risk at a genome-wide significance level of P < 5 × 10(-8) with the most significant association with rs4430796 (P = 1.62 × 10(-24)). 21576123

2011

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE After adjustments for age, the C allele of rs6983561 and the A allele of rs4430796 were significantly more frequent among the SPCa patients than among the controls. 21557267

2011

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE We identified an endometrial cancer susceptibility locus close to HNF1B at 17q12 (rs4430796, P = 7.1 × 10(-10)) that is also associated with risk of prostate cancer and is inversely associated with risk of type 2 diabetes. 21499250

2011

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Three HNF1B SNPS, rs11649743, rs4430796, and rs7501939, were associated with decreased risk of prostate cancer and were also associated, with marginal statistical significance, with increased risk of diabetes. 19998368

2010

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE These associations remained significant after excluding HNF1B SNP rs4430796 (a known PCa risk factor) from the analysis. 20203524

2010

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE The per-T2D-risk-allele odds ratios (95% confidence intervals) for rs4430796 were 0.79 (0.76, 0.83)] per G allele for prostate cancer (p<10(-15) for both); and 1.03 (0.99, 1.07) for all other cancers. 20526366

2010

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Recent studies have identified 2 distinct genetic variants along chromosome 17, including allele T of single nucleotide polymorphism rs4430796 on 17q12 and allele G of single nucleotide polymorphism rs1859962 on 17q24, that have been linked to prostate cancer risk. 19371897

2009

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Specifically, we sought to evaluate for effect modification between DM, a newly discovered prostate cancer susceptibility locus on chromosome 17q12 (single nucleotide polymorphism rs4430796) and prostate cancer features. 19627283

2009

dbSNP: rs4430796
rs4430796
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.800 GeneticVariation BEFREE Notably, rs4430796 was significantly associated with prostate cancer among men diagnosed at an early (<50 years) but not later age (P = 0.006 versus P = 0.118). 18701471

2008