RS886039453 WNT10A

Health Risk Chr 2:218890349
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What This Variant Does
"CLNSIG=5
Associated Conditions
Odonto-onycho-dermal dysplasia
Tooth agenesis
selective
4
Inborn genetic diseases
Schöpf-Schulz-Passarge syndrome
WNT10A-related disorder
Ectodermal dysplasia WNT10A related
Odonto-onycho-dermal dysplasia
Tooth agenesis
selective
4
Inborn genetic diseases
Schöpf-Schulz-Passarge syndrome
WNT10A-related disorder
Other Variants in WNT10A
rs121908118 rs121908119 rs121908120 rs121908121 rs121908122 rs121908123 rs146902156 rs318240759 rs147680216 rs368280129
Ask Dr. Hemsworth about this variant