List of variants in gene RYR1 reported as benign for RYR1-related myopathy

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.1077T>C (p.Ala359=)	rs10406027	0.90489
NM_000540.3(RYR1):c.-108T>C	rs4632259	0.04408
NM_000540.3(RYR1):c.2677G>A (p.Gly893Ser)	rs147336515	0.00202
NM_000540.3(RYR1):c.7025A>G (p.Asn2342Ser)	rs147213895	0.00104

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