Gene: HNF1B ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs757210
rs757210
HNF1B
A 0.710 GeneticVariation GWASCAT Identification of six new susceptibility loci for invasive epithelial ovarian cancer. 25581431

2015
dbSNP: rs757210
rs757210
HNF1B
0.710 GeneticVariation BEFREE We validated the two loci at 3q25 and 17q21 that were previously found to have associations close to genome-wide significance and identified three loci newly associated with risk: two loci associated with all EOC subtypes at 8q21 (rs11782652, P = 5.5 × 10(-9)) and 10p12 (rs1243180, P = 1.8 × 10(-8)) and another locus specific to the serous subtype at 17q12 (rs757210, P = 8.1 × 10(-10)). 23535730

2013
dbSNP: rs11651755
rs11651755
HNF1B
0.010 GeneticVariation BEFREE Different single-nucleotide polymorphisms associate with invasive serous (rs7405776 odds ratio (OR)=1.13, P=3.1 × 10(-10)) and clear cell (rs11651755 OR=0.77, P=1.6 × 10(-8)) epithelial ovarian cancer. 23535649

2013
dbSNP: rs7405776
rs7405776
HNF1B
0.010 GeneticVariation BEFREE Different single-nucleotide polymorphisms associate with invasive serous (rs7405776 odds ratio (OR)=1.13, P=3.1 × 10(-10)) and clear cell (rs11651755 OR=0.77, P=1.6 × 10(-8)) epithelial ovarian cancer. 23535649

2013