Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs605059
rs605059
Entrez Id: 3292;108783654
Gene Symbol: HSD17B1;LOC108783654
HSD17B1;LOC108783654
CUI: C0476089
Disease:
Endometrial Carcinoma
0.030 GeneticVariation BEFREE The result showed no significant association between HSD17B1 rs605059 gene polymorphisms and risks of endometrial cancer (AA vs. AG+GG: OR = 1.11, 95% CI = 0.94-1.32; AA+AG vs. GG: OR = 1.79, 95% CI = 0.42-7.52; AG vs. AA+ GG: OR = 0.87, 95% CI = 0.76-1.00; AA vs. GG: OR = 1.43, 95% CI = 0.62-3.30; A vs. G: OR = 1.00, 95% CI = 0.91-1.11) or endometriosis (AA vs. AG+GG: OR = 0.99, 95% CI = 0.75-1.32; AA+AG vs. GG: OR = 1.73, 95% CI = 0.92-3.25; AG vs. AA+ GG: OR = 1.24, 95% CI = 1.00-1.53; AA vs. GG: OR = 1.54, 95% CI = 0.79-2.97; A vs. G: OR = 1.23, 95% CI = 0.90-1.68). 26261478 2015
dbSNP: rs605059
rs605059
Entrez Id: 3292;108783654
Gene Symbol: HSD17B1;LOC108783654
HSD17B1;LOC108783654
CUI: C0476089
Disease:
Endometrial Carcinoma
0.030 GeneticVariation BEFREE We also found that among premenopausal women soy isoflavone intake significantly interacted with the rs605059 genotype in relation to endometrial cancer and that the inverse association between soy isoflavone intake and endometrial cancer only appeared among those with at least one A allele of the rs605059 polymorphism. 17301695 2007
dbSNP: rs605059
rs605059
Entrez Id: 3292;108783654
Gene Symbol: HSD17B1;LOC108783654
HSD17B1;LOC108783654
CUI: C0476089
Disease:
Endometrial Carcinoma
0.030 GeneticVariation BEFREE We identified and genotyped two haplotype-tagging SNPs (+1004C/T and +1322C/A), and genotyped an additional SNP [+1954A/G (Ser312Gly)] in nested case-control studies of endometrial cancer (cases = 222, controls = 666) and breast cancer (cases = 1007, controls = 1441) in the prospective Nurses' Health Study. 14973105 2004