WNT3A, Wnt family member 3A, 89780

N. diseases: 141; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs708122
rs708122
Entrez Id: 89780
Gene Symbol: WNT3A
WNT3A
CUI: C0005612
Disease:
Birth Weight
C 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs3121310
rs3121310
Entrez Id: 89780
Gene Symbol: WNT3A
WNT3A
CUI: C0810364
Disease:
Cleft Lip with or without Cleft Palate
0.010 GeneticVariation BEFREE No significant association was observed between the rs752107 and rs3121310 variants and risk/protection of nonsyndromic cleft lip with or without cleft palate. 29356097 2018
dbSNP: rs145882986
rs145882986
Entrez Id: 89780
Gene Symbol: WNT3A
WNT3A
CUI: C0019569
Disease:
Hirschsprung Disease
0.010 GeneticVariation 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
dbSNP: rs192966556
rs192966556
Entrez Id: 89780
Gene Symbol: WNT3A
WNT3A
CUI: C0019569
Disease:
Hirschsprung Disease
0.010 GeneticVariation 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
dbSNP: rs763783027
rs763783027
Entrez Id: 89780
Gene Symbol: WNT3A
WNT3A
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis
0.010 GeneticVariation BEFREE We determined the expression of Wnt3a, β-catenin, and Cyclin D1 in the adult spinal cord of SOD1(G93A) ALS transgenic mice at different stages by RT-PCR, Western blot, and immunofluorescence labeling techniques. 22426476 2012