List of variants reported as likely benign for Congenital myopathy with fiber type disproportion

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_152263.4(TPM3):c.*3248G>A	rs12026177	0.15247
NM_152263.4(TPM3):c.*389G>A	rs74731791	0.01922
NM_152263.4(TPM3):c.*4333A>G	rs34629044	0.01027
NM_152263.4(TPM3):c.*780A>G	rs185779007	0.00287
NM_152263.4(TPM3):c.*5640C>T	rs564296987	0.00257
NM_152263.4(TPM3):c.*4876C>T	rs141628385	0.00178
NM_152263.4(TPM3):c.*157C>T	rs144482403	0.00047
NM_152263.4(TPM3):c.*1077A>C	rs557217738	0.00045
NM_152263.4(TPM3):c.*2138T>C	rs566002553	0.00031
NM_152263.4(TPM3):c.*5701C>T	rs373631033	0.00018
NM_001100.4(ACTA1):c.454+3G>T	rs200976037	0.00001
NM_152263.4(TPM3):c.*1152C>T	rs535068015	0.00001
NM_152263.4(TPM3):c.*4940C>G	rs562373211	0.00001
NM_001100.4(ACTA1):c.108C>T (p.Ile36=)	rs143948837
NM_001100.4(ACTA1):c.809-13dup	rs201427429
NM_152263.4(TPM3):c.1246_1247dup	rs72189266
NM_152263.4(TPM3):c.*2147del	rs68185418
NM_152263.4(TPM3):c.*5594G>T	rs550606876

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