Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12700667
rs12700667 		A 0.820 GeneticVariation GWASCAT Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism. 28537267

2017
dbSNP: rs12700667
rs12700667 		0.820 GeneticVariation BEFREE The study suggests that the endometriosis-associated genetic polymorphisms (rs12700667) from GWAS be associated with the risk of developing ovarian endometriosis in North Chinese women. 27233752

2017
dbSNP: rs12700667
rs12700667 		0.820 GeneticVariation GWASCAT Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis. 28333195

2017
dbSNP: rs12700667
rs12700667 		A 0.820 GeneticVariation GWASCAT Genome-wide association meta-analysis identifies new endometriosis risk loci. 23104006

2012
dbSNP: rs12700667
rs12700667 		A 0.820 GeneticVariation GWASDB Genome-wide association meta-analysis identifies new endometriosis risk loci. 23104006

2012
dbSNP: rs12700667
rs12700667 		A 0.820 GeneticVariation GWASCAT We replicated rs12700667 in an independent cohort from the United States of 2,392 self-reported, surgically confirmed endometriosis cases and 2,271 controls (P = 1.2 × 10⁻³, OR = 1.17, 95% CI 1.06-1.28), resulting in a genome-wide significant P value of 1.4 × 10⁻⁹ (OR = 1.20, 95% CI 1.13-1.27) for 'all' endometriosis in our combined datasets of 5,586 cases and 9,331 controls. rs12700667 is located in an intergenic region upstream of the plausible candidate genes NFE2L3 and HOXA10. 21151130

2011
dbSNP: rs12700667
rs12700667 		0.820 GeneticVariation BEFREE The strongest association signal was on 7p15.2 (rs12700667) for 'all' endometriosis (P = 2.6 × 10⁻⁷, odds ratio (OR) = 1.22, 95% CI 1.13-1.32) and for moderate to severe disease (P = 1.5 × 10⁻⁹, OR = 1.38, 95% CI 1.24-1.53). 21151130

2011
dbSNP: rs12700667
rs12700667 		A 0.820 GeneticVariation GWASDB We replicated rs12700667 in an independent cohort from the United States of 2,392 self-reported, surgically confirmed endometriosis cases and 2,271 controls (P = 1.2 × 10⁻³, OR = 1.17, 95% CI 1.06-1.28), resulting in a genome-wide significant P value of 1.4 × 10⁻⁹ (OR = 1.20, 95% CI 1.13-1.27) for 'all' endometriosis in our combined datasets of 5,586 cases and 9,331 controls. rs12700667 is located in an intergenic region upstream of the plausible candidate genes NFE2L3 and HOXA10. 21151130

2011