Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908119
rs121908119
WNT10A ; LOC107984111
A 0.700 CausalMutation CLINVAR Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype study. 28105635

2017
dbSNP: rs121908119
rs121908119
WNT10A ; LOC107984111
A 0.700 CausalMutation CLINVAR Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions. 25356970

2015
dbSNP: rs121908119
rs121908119
WNT10A ; LOC107984111
A 0.700 CausalMutation CLINVAR The WNT10A gene in ectodermal dysplasias and selective tooth agenesis. 24700731

2014
dbSNP: rs121908119
rs121908119
WNT10A ; LOC107984111
A 0.700 CausalMutation CLINVAR WNT10A variants are associated with non-syndromic tooth agenesis in the general population. 24043634

2014
dbSNP: rs121908119
rs121908119
WNT10A ; LOC107984111
A 0.700 CausalMutation CLINVAR WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes. 19559398

2009
dbSNP: rs121908119
rs121908119
WNT10A ; LOC107984111
A 0.700 CausalMutation CLINVAR Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. 17847007

2007