WNT3A, Wnt family member 3A, 89780

N. diseases: 141; N. variants: 5
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease
0.310 GeneticVariation disease BEFREE Consequently, when rs192966556 and rs145882986 alleles of the WNT3A gene lack the SNPs, they are especially associated with a greater risk of HSCR (OR [95% confidence interval]=1.791, p=0.001; OR [95% confidence interval]=1.556, p=0.003, respectively). 24817932 2014
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease
0.310 Biomarker disease GENOMICS_ENGLAND The present study aims to detect the interactions of genetic variations in the WNT3A gene and examine the biological expression levels with Hirschsprung disease (HSCR) in the Chinese people. 24817932 2014