List of variants in gene RYR1 reported as pathogenic by Juno Genomics, Hangzhou Juno Genomics, Inc

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_000540.3(RYR1):c.7360C>T (p.Arg2454Cys)	rs193922816	0.00001
NM_000540.3(RYR1):c.14762T>C (p.Phe4921Ser)	rs118192156
NM_000540.3(RYR1):c.742G>C (p.Gly248Arg)	rs1801086

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