ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.1232-12del

dbSNP: rs752301693
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002541287 SCV002952304 benign Myofibrillar myopathy 4 2023-07-10 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001795528 SCV002034644 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001796930 SCV002037323 likely benign not provided no assertion criteria provided clinical testing

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