ClinVar Miner

Submissions for variant NM_001368067.1(LDB3):c.414C>T (p.Ile138=)

dbSNP: rs372423575
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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 RCV001405588 SCV001607519 likely benign Myofibrillar myopathy 4 2023-10-14 criteria provided, single submitter clinical testing

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