List of variants in gene MYOZ2 reported as uncertain significance by Clinical Genetics, Academic Medical Center

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_016599.5(MYOZ2):c.479C>T (p.Pro160Leu)	rs200791464	0.00008
NM_016599.5(MYOZ2):c.148C>T (p.Leu50Phe)	rs1015335570	0.00001
NM_016599.5(MYOZ2):c.712G>A (p.Gly238Arg)	rs796785947	0.00001

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