RS121908119 WNT10A
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What This Variant Does
"[OMIM:?]
Associated Conditions
Odonto-onycho-dermal dysplasia
Schöpf-Schulz-Passarge syndrome
Tooth agenesis
selective
4
Inborn genetic diseases
WNT10A-related disorder
Ectodermal dysplasia
Ectodermal dysplasia WNT10A related
Odonto-onycho-dermal dysplasia
Schöpf-Schulz-Passarge syndrome
Tooth agenesis
selective
4
Inborn genetic diseases
Other Variants in WNT10A