Variants in gene RYR1 with conflicting interpretations "likely benign" and "likely pathogenic"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.6721C>T (p.Arg2241Ter)	rs200563280	0.00013
NM_000540.3(RYR1):c.2366G>A (p.Arg789Gln)	rs200069592	0.00011
NM_000540.3(RYR1):c.12406C>A (p.Arg4136Ser)	rs193922849	0.00001
NM_000540.3(RYR1):c.4481T>C (p.Val1494Ala)	rs767928113
NM_000540.3(RYR1):c.5628GGA[2] (p.Glu1878del)	rs371047178
NM_000540.3(RYR1):c.6353G>C (p.Arg2118Pro)	rs201649680

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