List of variants in gene CASK reported as benign for not specified

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001367721.1(CASK):c.1034-6C>T	rs73470569	0.09241
NM_001367721.1(CASK):c.2039+15G>A	rs41307351	0.00602
NM_001367721.1(CASK):c.2040-9A>G	rs138290714	0.00595
NM_001367721.1(CASK):c.363T>C (p.Tyr121=)	rs41431245	0.00591
NM_001367721.1(CASK):c.1125C>T (p.Phe375=)	rs141790702	0.00424
NM_001367721.1(CASK):c.1233+18T>C	rs199794978	0.00230
NM_001367721.1(CASK):c.1077G>A (p.Ala359=)	rs145641295	0.00084
NM_001367721.1(CASK):c.2442G>A (p.Ala814=)	rs141158465	0.00013
NM_001367721.1(CASK):c.1669-9C>A	rs562152407	0.00003
NM_001367721.1(CASK):c.2019T>G (p.Pro673=)	rs546044640	0.00001
NM_001367721.1(CASK):c.1504-6dup	rs749321162
NM_001367721.1(CASK):c.2198A>G (p.Lys733Arg)	rs587783363
NM_001367721.1(CASK):c.2521-11dup	rs199560653
NM_001367721.1(CASK):c.2521-2A>T	rs398122845
NM_001367721.1(CASK):c.2569A>G (p.Ile857Val)	rs2147067640
NM_001367721.1(CASK):c.430-31TGTT[2]	rs200962618
NM_001367721.1(CASK):c.891A>G (p.Lys297=)	rs544979992

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