ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.1677-11T>C

gnomAD frequency: 0.00001  dbSNP: rs779076719
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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 RCV002171470 SCV002477585 likely benign Myofibrillar myopathy 4 2024-02-26 criteria provided, single submitter clinical testing

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