List of variants in gene RYR2 reported as uncertain significance by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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_001035.3(RYR2):c.6299G>A (p.Arg2100Gln)	rs796202631	0.00004
NM_001035.3(RYR2):c.13804C>T (p.Arg4602Ter)	rs878853077
NM_001035.3(RYR2):c.1775G>T (p.Gly592Val)	rs794728724

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