List of variants in gene RYR1 reported as uncertain significance by Daryl Scott Lab, Baylor College of Medicine

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.7204C>T (p.Arg2402Trp)	rs575780192	0.00005
NM_000540.3(RYR1):c.8991C>A (p.Phe2997Leu)	rs1377413977	0.00001
NM_000540.3(RYR1):c.9472+9G>A	rs1392237616	0.00001

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