ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.5923-8T>C

dbSNP: rs2148596590
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002160505 SCV002422694 likely benign Duchenne muscular dystrophy 2020-11-16 criteria provided, single submitter clinical testing

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