List of variants reported as benign for RYR1-related myopathy by ClinGen Congenital Myopathies Variant Curation Expert Panel, ClinGen

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.1077T>C (p.Ala359=)	rs10406027	0.90489
NM_000540.3(RYR1):c.8589T>C (p.Ser2863=)	rs2229146	0.32548
NM_000540.3(RYR1):c.8400+28A>G	rs2915953	0.32146
NM_000540.3(RYR1):c.-108T>C	rs4632259	0.04408
NM_000540.3(RYR1):c.2677G>A (p.Gly893Ser)	rs147336515	0.00202
NM_000540.3(RYR1):c.7025A>G (p.Asn2342Ser)	rs147213895	0.00104

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