List of variants reported as likely pathogenic for Central core myopathy by Laboratory of Medical Genetics, National & Kapodistrian University of Athens

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.4711A>G (p.Ile1571Val)	rs146429605	0.00107
NM_000540.3(RYR1):c.10097G>A (p.Arg3366His)	rs137932199	0.00073
NM_000540.3(RYR1):c.1250T>C (p.Leu417Pro)	rs764262446	0.00004
NM_000540.3(RYR1):c.1264G>A (p.Gly422Arg)	rs757157750	0.00002
NM_000540.3(RYR1):c.6445G>A (p.Val2149Met)	rs776830747	0.00001

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