rs11263763, HNF1B

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
0.800 GeneticVariation GWASCAT Five endometrial cancer risk loci identified through genome-wide association analysis. 27135401 2016
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
0.800 GeneticVariation GWASDB Genome-wide association study identifies a common variant associated with risk of endometrial cancer. 21499250 2011
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
0.700 GeneticVariation GWASCAT A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences. 26034056 2015
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation GWASDB Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. 22885922 2012
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
0.010 GeneticVariation BEFREE SNP rs11263763 genotype was associated with HNF1B mRNA expression but not with HNF1B methylation in endometrial tumor samples from The Cancer Genome Atlas. 25378557 2015
Endometrial Neoplasms
CUI: C0014170
Disease: Endometrial Neoplasms
0.010 GeneticVariation BEFREE SNP rs11263763 genotype was associated with HNF1B mRNA expression but not with HNF1B methylation in endometrial tumor samples from The Cancer Genome Atlas. 25378557 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
0.010 GeneticVariation BEFREE SNP rs11263763 genotype was associated with HNF1B mRNA expression but not with HNF1B methylation in endometrial tumor samples from The Cancer Genome Atlas. 25378557 2015