List of variants reported as likely pathogenic for childhood-onset nemaline myopathy by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001100.4(ACTA1):c.347C>T (p.Ala116Val)	rs1659975747
NM_001100.4(ACTA1):c.769T>C (p.Phe257Leu)
NM_003289.4(TPM2):c.782A>G (p.Tyr261Cys)	rs1824676022

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