List of variants reported as likely benign for cap myopathy by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_152263.4(TPM3):c.*4062G>A	rs140590273	0.00864
NM_152263.4(TPM3):c.*5149G>A	rs78002555	0.00816
NM_152263.4(TPM3):c.92A>C (p.Lys31Thr)	rs62000429	0.00596
NM_152263.4(TPM3):c.*4154C>T	rs145053113	0.00572
NM_152263.4(TPM3):c.*3497T>C	rs144544045	0.00465
NM_152263.4(TPM3):c.*878A>G	rs116789181	0.00321
NM_152263.4(TPM3):c.*780A>G	rs185779007	0.00287
NM_152263.4(TPM3):c.*4876C>T	rs141628385	0.00178
NM_152263.4(TPM3):c.*2138T>C	rs566002553	0.00031
NM_152263.4(TPM3):c.*5701C>T	rs373631033	0.00018
NM_152263.4(TPM3):c.*4940C>G	rs562373211	0.00001
NM_152263.4(TPM3):c.*1130C>T	rs143058197

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