List of variants in gene CASQ1 reported as likely benign for hereditary skeletal muscle 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001231.5(CASQ1):c.364+9G>T	rs115023646	0.00505
NM_001231.5(CASQ1):c.1018G>A (p.Asp340Asn)	rs749145120	0.00010

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