List of variants in gene SQSTM1 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_003900.5(SQSTM1):c.984G>A (p.Ser328=)	rs146164139	0.00374
NM_003900.5(SQSTM1):c.1176G>A (p.Pro392=)	rs75700262	0.00052

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