List of variants in gene DCX reported as benign for not provided

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001195553.2(DCX):c.-22-312_-22-306del	rs200417598	0.07837
NM_001195553.2(DCX):c.808+284C>G	rs17222328	0.05268
NM_001195553.2(DCX):c.705+29G>A	rs61036541	0.01792
NM_001195553.2(DCX):c.1044+132G>C	rs10482456	0.01551
NM_001195553.2(DCX):c.588T>C (p.Arg196=)	rs138706968	0.00376
NM_001195553.2(DCX):c.809-9T>C	rs199537326	0.00073
NM_001195553.2(DCX):c.96C>T (p.Ser32=)	rs148472336	0.00060
NM_001195553.2(DCX):c.666C>T (p.Thr222=)	rs143501582	0.00032
NM_001195553.2(DCX):c.856G>T (p.Ala286Ser)	rs149495971	0.00032
NM_001195553.2(DCX):c.948A>C (p.Ala316=)	rs770799939	0.00008
NM_001195553.2(DCX):c.339C>A (p.Ile113=)	rs587783543	0.00001
NM_001195553.2(DCX):c.1044+234G>A	rs41311727
NM_001195553.2(DCX):c.1045-14T>C
NM_001195553.2(DCX):c.706-4A>G
NM_001195553.2(DCX):c.936C>T (p.Asn312=)

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