ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.5196C>T (p.Asp1732=)

dbSNP: rs2147234471
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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 RCV001394677 SCV001596367 likely benign Duchenne muscular dystrophy 2020-01-17 criteria provided, single submitter clinical testing

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