Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs202024965
rs202024965
WNT10A
0.700 GeneticVariation UNIPROT Role of WNT10A in failure of tooth development in humans and zebrafish. 29178643

2017
dbSNP: rs202024965
rs202024965
WNT10A
0.700 GeneticVariation UNIPROT Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients. 27657131

2016
dbSNP: rs202024965
rs202024965
WNT10A
0.700 GeneticVariation UNIPROT WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations. 24449199

2014
dbSNP: rs202024965
rs202024965
WNT10A
0.700 GeneticVariation UNIPROT WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity. 24311251

2014
dbSNP: rs202024965
rs202024965
WNT10A
0.700 GeneticVariation UNIPROT Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia. 23401279

2013
dbSNP: rs202024965
rs202024965
WNT10A
0.700 GeneticVariation UNIPROT Mutations in WNT10A are present in more than half of isolated hypodontia cases. 22581971

2012
dbSNP: rs202024965
rs202024965
WNT10A
0.700 GeneticVariation UNIPROT WNT10A and isolated hypodontia. 21484994

2011
dbSNP: rs202024965
rs202024965
WNT10A
0.700 GeneticVariation UNIPROT Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases. 20979233

2011