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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DLX3
(D246H)
Single nucleotide variant
(missense variant)
Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism
+2 more
GBenign
DLX3
(Y237C)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
DLX3
(G191fs)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic
DLX3
(A90S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
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