RS387906405 DLX3
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What This Variant Does
"CLNSIG=5
Associated Conditions
Tricho-dento-osseous syndrome
DLX3-related disorder
Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism
Inborn genetic diseases
Tricho-dento-osseous syndrome
DLX3-related disorder
Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism
Inborn genetic diseases
Other Variants in DLX3