List of variants in gene DLX3 reported as likely benign for tooth hard tissue disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_005220.3(DLX3):c.832G>A (p.Gly278Arg)	rs151180891	0.00067
NM_005220.3(DLX3):c.82G>T (p.Asp28Tyr)	rs147702169	0.00058
NM_005220.3(DLX3):c.-37C>G	rs375929276	0.00029
NM_005220.3(DLX3):c.*1328T>G	rs568427405	0.00014
NM_005220.3(DLX3):c.636A>G (p.Ser212=)	rs759832786	0.00002
NM_005220.3(DLX3):c.465G>A (p.Ala155=)	rs534788536

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