Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11263763
rs11263763
HNF1B
A 0.800 GeneticVariation GWASCAT Five endometrial cancer risk loci identified through genome-wide association analysis. 27135401

2016
dbSNP: rs11651052
rs11651052
HNF1B
0.800 GeneticVariation GWASCAT GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer. 27008869

2016
dbSNP: rs11263763
rs11263763
HNF1B
0.800 GeneticVariation GWASDB Genome-wide association study identifies a common variant associated with risk of endometrial cancer. 21499250

2011
dbSNP: rs11651052
rs11651052
HNF1B
0.800 GeneticVariation GWASDB Genome-wide association study identifies a common variant associated with risk of endometrial cancer. 21499250

2011
dbSNP: rs4430796
rs4430796
HNF1B
0.730 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
HNF1B
0.730 GeneticVariation BEFREE rs4430796 polymorphism of HNF1B gene influences independently the prognosis of EC patients with a potential effect on tumor chemo-sensitivity. 25885815

2015
dbSNP: rs4430796
rs4430796
HNF1B
A 0.730 GeneticVariation GWASDB 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
HNF1B
0.730 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: rs1740828
rs1740828 		G 0.710 GeneticVariation GWASCAT Identification of nine new susceptibility loci for endometrial cancer. 30093612

2018
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
C 0.710 GeneticVariation GWASCAT Identification of nine new susceptibility loci for endometrial cancer. 30093612

2018
dbSNP: rs1740828
rs1740828 		0.710 GeneticVariation GWASCAT We describe one new locus reaching genome-wide significance (P < 5 × 10 <sup>-</sup><sup>8</sup>) at 6p22.3 (rs1740828; P = 2.29 × 10 <sup>-</sup><sup>8</sup>, OR = 1.20), providing evidence of an additional region of interest for genetic susceptibility to endometrial cancer. 27008869

2016
dbSNP: rs1740828
rs1740828 		0.710 GeneticVariation BEFREE We describe one new locus reaching genome-wide significance (P < 5 × 10 <sup>-</sup><sup>8</sup>) at 6p22.3 (rs1740828; P = 2.29 × 10 <sup>-</sup><sup>8</sup>, OR = 1.20), providing evidence of an additional region of interest for genetic susceptibility to endometrial cancer. 27008869

2016
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
0.710 GeneticVariation BEFREE A combined analysis revealed one genome-wide significant polymorphism, rs3184504, on chromosome 12q24 (OR = 1.10, P = 7.23 × 10(-9)) with shared effects on CRC and EC risk. 26621817

2015
dbSNP: rs7501939
rs7501939
HNF1B
0.710 GeneticVariation BEFREE Rs4430796 and rs7501939 were associated with endometrial cancer risk in MEC and WHI with no heterogeneity observed across racial/ethnic groups (P ≥ 0.21) or between studies (P ≥ 0.70). 22299039

2012
dbSNP: rs7501939
rs7501939
HNF1B
0.710 GeneticVariation GWASDB Genome-wide association study identifies a common variant associated with risk of endometrial cancer. 21499250

2011
dbSNP: rs79184941
rs79184941
FGFR2
0.710 GeneticVariation BEFREE FGFR2 exons 7 and 12 unlabeled DNA probes allow for easy screening of endometrial carcinoma for the 2 most common FGFR2 mutations (S252W and N550K). 21285871

2011
dbSNP: rs17879961
rs17879961
CHEK2
0.710 GeneticVariation BEFREE This study is the first to explore the association between germline CHEK2 I157T and EC. 18834326

2009
dbSNP: rs17879961
rs17879961
CHEK2
G 0.710 GeneticVariation CLINVAR

dbSNP: rs79184941
rs79184941
FGFR2
C 0.710 CausalMutation CLINVAR

dbSNP: rs10835920
rs10835920 		T 0.700 GeneticVariation GWASCAT Identification of nine new susceptibility loci for endometrial cancer. 30093612

2018
dbSNP: rs10850382
rs10850382
LOC107984437
T 0.700 GeneticVariation GWASCAT Identification of nine new susceptibility loci for endometrial cancer. 30093612

2018
dbSNP: rs11263761
rs11263761
HNF1B
A 0.700 GeneticVariation GWASCAT Identification of nine new susceptibility loci for endometrial cancer. 30093612

2018
dbSNP: rs1129506
rs1129506
EVI2A ; NF1
G 0.700 GeneticVariation GWASCAT Identification of nine new susceptibility loci for endometrial cancer. 30093612

2018
dbSNP: rs113998067
rs113998067 		C 0.700 GeneticVariation GWASCAT Identification of nine new susceptibility loci for endometrial cancer. 30093612

2018
dbSNP: rs11583244
rs11583244 		T 0.700 GeneticVariation GWASCAT Identification of nine new susceptibility loci for endometrial cancer. 30093612

2018