List of variants in gene RYR2 reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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_001035.3(RYR2):c.8209-3A>G	rs376788358	0.00047
NM_001035.3(RYR2):c.2573C>T (p.Thr858Met)	rs377068202	0.00006
NM_001035.3(RYR2):c.14246G>T (p.Gly4749Val)	rs1558457775
NM_001035.3(RYR2):c.14383A>G (p.Lys4795Glu)	rs1558462911

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