ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.72C>T (p.Asn24=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003612141 SCV004531093 likely benign Myofibrillar myopathy 4 2024-11-13 criteria provided, single submitter clinical testing

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