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

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 4

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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.10648C>T (p.Arg3550Trp)	rs536304635	0.00008
NM_000540.3(RYR1):c.11763C>A (p.Tyr3921Ter)	rs377178986	0.00004
NM_000540.3(RYR1):c.9571G>A (p.Gly3191Arg)	rs756331568	0.00001

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