List of variants in gene DCX reported as likely benign by GeneDx

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001195553.2(DCX):c.947-46T>C	rs113181679	0.01340
NM_001195553.2(DCX):c.705+48A>G	rs201805884	0.00836
NM_001195553.2(DCX):c.705+95C>T	rs146900657	0.00535
NM_001195553.2(DCX):c.*273C>T	rs111957035	0.00508
NM_001195553.2(DCX):c.808+224C>T	rs144344521	0.00388
NM_001195553.2(DCX):c.946+275C>G	rs188874241	0.00387
NM_001195553.2(DCX):c.96C>T (p.Ser32=)	rs148472336	0.00060

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