ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.93+7G>T

dbSNP: rs397517229
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000038773 SCV000062451 likely benign not specified 2008-11-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003611495 SCV004526795 likely benign Myofibrillar myopathy 4 2023-11-30 criteria provided, single submitter clinical testing

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