ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.6117+15C>T

gnomAD frequency: 0.00006  dbSNP: rs754718247
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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 RCV002161449 SCV002475975 likely benign Duchenne muscular dystrophy 2024-11-18 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500359 SCV002806602 likely benign Becker muscular dystrophy; Duchenne muscular dystrophy; Dilated cardiomyopathy 3B 2021-09-01 criteria provided, single submitter clinical testing

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