List of variants reported as uncertain significance for Central core myopathy; Malignant hyperthermia, susceptibility to, 1; Congenital multicore myopathy with external ophthalmoplegia; King Denborough syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.11798A>G (p.Tyr3933Cys)	rs147136339	0.00108
NM_000540.3(RYR1):c.10097G>A (p.Arg3366His)	rs137932199	0.00073
NM_000540.3(RYR1):c.9148G>A (p.Val3050Ile)	rs200797340	0.00014
NM_000540.3(RYR1):c.13207G>A (p.Ala4403Thr)	rs1051206491	0.00003
NM_000540.3(RYR1):c.7099G>A (p.Ala2367Thr)	rs146306934	0.00003
NM_000540.3(RYR1):c.10735G>A (p.Val3579Ile)	rs764650501	0.00001
NM_000540.3(RYR1):c.1297A>G (p.Thr433Ala)
NM_000540.3(RYR1):c.13471C>G (p.Pro4491Ala)
NM_000540.3(RYR1):c.4589C>G (p.Ala1530Gly)
NM_000540.3(RYR1):c.4592A>G (p.Asn1531Ser)	rs1968860939

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