List of variants reported as likely pathogenic for congenital myopathy by DASA

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.24114+1G>A	rs755239192	0.00009
NM_017534.6(MYH2):c.2725G>T (p.Glu909Ter)	rs780124402	0.00002
NM_032608.7(MYO18B):c.2626C>T (p.Arg876Ter)	rs267606197

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