List of variants reported as likely pathogenic for congenital myopathy by Johns Hopkins Genomics, Johns Hopkins University

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.102214T>C (p.Trp34072Arg)	rs375159973	0.00002
NC_012920.1(MT-ND5):m.12923G>A
NM_001267550.2(TTN):c.20449del (p.Ser6817fs)	rs2079254006
NM_001267550.2(TTN):c.826C>T (p.Gln276Ter)	rs2154358498

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