List of variants in gene DLX3 reported as benign for bone disorder

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.516+23C>T	rs2303467	0.18480
NM_005220.3(DLX3):c.402G>A (p.Thr134=)	rs2303466	0.18221
NM_005220.3(DLX3):c.138C>T (p.Pro46=)	rs33937843	0.08182

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