ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.94-20C>T

dbSNP: rs779928559
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002539694 SCV003440994 likely benign Myofibrillar myopathy 4 2024-01-25 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001700871 SCV001923926 benign not specified no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001726640 SCV001963301 likely benign not provided no assertion criteria provided clinical testing

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