List of variants in gene RYR1 reported as likely pathogenic for 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.2654G>A (p.Arg885His)	rs370634440	0.00013
NM_000540.3(RYR1):c.3235_3240dup (p.Ser1079_Tyr1080dup)	rs797045933	0.00001

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