ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.3942A>G (p.Arg1314=)

dbSNP: rs2098269367
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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 RCV001469397 SCV001673477 likely benign Duchenne muscular dystrophy 2024-05-25 criteria provided, single submitter clinical testing

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