Variant: rs11651052 

    present in Gene: HNF1B
    present in Chromosome: 17
    Position on Chromosome: 37742390
    Alleles of this Variant: G/A

rs11651052 in HNF1B gene and Benign Prostatic Hyperplasia PMID 30410027 2018 Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.

rs11651052 in HNF1B gene and Body mass index PMID 28892062 2017 Genome-wide association study identifies 112 new loci for body mass index in the Japanese population.

rs11651052 in HNF1B gene and Diabetes Mellitus, Non-Insulin-Dependent PMID 22885922 2012 Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.

PMID 30718926 2019 Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population.

rs11651052 in HNF1B gene and Endometrial Carcinoma PMID 21499250 2011 Genome-wide association study identifies a common variant associated with risk of endometrial cancer.

PMID 27008869 2016 GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer.

rs11651052 in HNF1B gene and Lower Urinary Tract Symptoms PMID 30410027 2018 Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.

rs11651052 in HNF1B gene and Prostate carcinoma PMID 30410027 2018 Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.

PMID 27262462 2016 Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.

rs11651052 in HNF1B gene and Prostate specific antigen measurement PMID 30410027 2018 Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.