"Genome-Nilou Lab"[submitter] AND "DLX3"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1221806	NM_005220.3(DLX3):c.516+23C>T	DLX3	Single nucleotide variant (intron variant)	Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism +2 more	GBenign
Select item 259676	NM_005220.3(DLX3):c.402G>A (p.Thr134=)	DLX3	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 259675	NM_005220.3(DLX3):c.138C>T (p.Pro46=)	DLX3	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign

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