However, considering the potential phenotypic contribution from sequence variants of other ectodermal dysplasia genes, we also analyzed EDA,EDAR, and EDARADD. The results identified four WNT10A sequence variations running in this family, g.6836C>A, c.321C>A, p.Cys107*; g.7008G>A, c.493G>A, p.Gly165Arg; g.14757T>A, c.682T>A, p.Phe228Ile; and g.15162A>C, c.1087A>C, p.Asn363His (Fig. S14). Here, WNT10A is linked to ectodermal dysplasia syndrome.