ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.3162+5T>C

gnomAD frequency: 0.00004  dbSNP: rs779431450
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001436769 SCV001639613 likely benign Duchenne muscular dystrophy 2025-01-15 criteria provided, single submitter clinical testing
GeneDx RCV001675992 SCV001894728 likely benign not provided 2020-12-08 criteria provided, single submitter clinical testing

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