Variant: rs121908120 

    present in Gene: WNT10A
    present in Chromosome: 2
    Position on Chromosome: 218890289
    Alleles of this Variant: T/A

rs121908120 in WNT10A gene and Acne Vulgaris PMID 30542056 2018 Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne.

rs121908120 in WNT10A gene and Central corneal thickness PMID 29760442 2018 Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.

PMID 30894546 2019 Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.

rs121908120 in WNT10A gene and Dental caries PMID 31235808 2019 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data.

rs121908120 in WNT10A gene and Developmental absence of tooth PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.

rs121908120 in WNT10A gene and Hypodontia PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.

rs121908120 in WNT10A gene and Hypodontia Oligodontia with Orofacial Cleft PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.

rs121908120 in WNT10A gene and Odontoonychodermal dysplasia PMID 24458874 2014 Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations.

PMID 17847007 2007 Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia.

PMID 28589954 2017 WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation.

PMID 19559398 2009 WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

PMID 19471313 2009 WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome.

rs121908120 in WNT10A gene and Oligodontia PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.

rs121908120 in WNT10A gene and Reduced number of teeth PMID 25629078 2015 Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.

rs121908120 in WNT10A gene and TOOTH AGENESIS, SELECTIVE, 4 (disorder) PMID 29178643 2017 Role of WNT10A in failure of tooth development in humans and zebrafish.

PMID 20979233 2011 Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.

PMID 24311251 2014 WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity.

PMID 27657131 2016 Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients.

PMID 22581971 2012 Mutations in WNT10A are present in more than half of isolated hypodontia cases.

PMID 23401279 2013 Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.

PMID 24449199 2014 WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations.

PMID 21484994 2011 WNT10A and isolated hypodontia.

rs121908120 in WNT10A gene and TOOTH AGENESIS, SELECTIVE, 9 PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.

rs121908120 in WNT10A gene and Tooth Agenesis, Familial PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.

rs121908120 in WNT10A gene and Tooth Agenesis, Selective, With Orofacial Cleft PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.

rs121908120 in WNT10A gene and Tooth development and eruption disorder PMID 29364747 2018 Rare and Common Variants Conferring Risk of Tooth Agenesis.