ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.690-20G>A

gnomAD frequency: 0.00002  dbSNP: rs371706056
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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 RCV001987605 SCV002220592 likely benign Myofibrillar myopathy 4 2023-07-22 criteria provided, single submitter clinical testing

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