Variant: rs372993798 

    present in Gene: WNT10A
    present in Chromosome: 2
    Position on Chromosome: 218889998
    Alleles of this Variant: G/A;T

rs372993798 in WNT10A gene and Odontoonychodermal dysplasia PMID 24902757 2014 Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

PMID 22670871 2013 Late diagnosis of ectodermal dysplasia syndrome.

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

PMID 21143469 2011 Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum.

rs372993798 in WNT10A gene and SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder) PMID 19559398 2009 WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

PMID 21143469 2011 Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum.

rs372993798 in WNT10A gene and TOOTH AGENESIS, SELECTIVE, 4 (disorder) PMID 21143469 2011 Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum.

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

PMID 22670871 2013 Late diagnosis of ectodermal dysplasia syndrome.

PMID 24902757 2014 Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.