Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Endometriosis
CUI: C0014175
Disease: Endometriosis
0.750 GeneticVariation BEFREE This might constitute the first step towards identifying polymorphism combinations that predispose to endometriosis (IFNG (CA) repeat, GSTM1 null genotype, GSTP1 rs1695, WNT4 rs16826658 and WNT4 rs2235529) in a large cohort of patients with well-defined inclusion criteria. 31821471 2020
Endometriosis
CUI: C0014175
Disease: Endometriosis
0.750 GeneticVariation BEFREE Our results suggested that rs16826658 and rs3820282 polymorphisms on WNT4 gene might be involved in the pathogenesis of endometriosis in the infertile women studied. 26139156 2015
Endometriosis
CUI: C0014175
Disease: Endometriosis
0.750 GeneticVariation BEFREE No significant association was found between endometriosis and rs7521902 (A/C), rs16826658 (G/T), or rs7515106 (C/T). 25682310 2015
Endometriosis
CUI: C0014175
Disease: Endometriosis
0.750 GeneticVariation BEFREE Our results suggest that the rs10965235 SNP in the CDKN2B-AS gene and the rs16826658 SNP near the WNT4 gene were significantly associated with endometriosis in this Korean population. 25154675 2014
Endometriosis
CUI: C0014175
Disease: Endometriosis
0.750 GeneticVariation GWASCAT Genome-wide association study link novel loci to endometriosis. 23472165 2013
Endometriosis
CUI: C0014175
Disease: Endometriosis
0.750 GeneticVariation BEFREE A SNP, rs16826658, in the LD block including WNT4 on chromosome 1p36, which is considered to play an important role in the development of the female genital tract, revealed a possible association with endometriosis (P = 1.66 x 10(-6), odds ratio = 1.20). 20601957 2010