List of variants in gene DLX3 reported as likely pathogenic for dental enamel hypoplasia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005220.3(DLX3):c.537C>A (p.Asn179Lys)
NM_005220.3(DLX3):c.574del (p.Glu192fs)	rs1057518764
NM_005220.3(DLX3):c.574dup (p.Glu192fs)	rs1057518764

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