List of variants in gene CASK reported as benign by Ambry Genetics

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: 9

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HGVS	dbSNP	gnomAD frequency
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.1077G>A (p.Ala359=)	rs145641295	0.00084
NM_001367721.1(CASK):c.1794C>T (p.Asn598=)	rs143991107	0.00072
NM_001367721.1(CASK):c.2297G>A (p.Arg766Gln)	rs137964936	0.00053
NM_001367721.1(CASK):c.2442G>A (p.Ala814=)	rs141158465	0.00013
NM_001367721.1(CASK):c.1922G>A (p.Arg641Lys)	rs76106850	0.00003
NM_001367721.1(CASK):c.2019T>G (p.Pro673=)	rs546044640	0.00001
NM_001367721.1(CASK):c.891A>G (p.Lys297=)	rs544979992

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