ClinVar Miner

Submissions for variant NM_001368067.1(LDB3):c.420G>C (p.Val140=)

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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 RCV003613214 SCV004504287 likely benign Myofibrillar myopathy 4 2023-03-09 criteria provided, single submitter clinical testing

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