ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.4311C>T (p.Ala1437=)

dbSNP: rs1410304028
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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 RCV001496530 SCV001701229 likely benign Duchenne muscular dystrophy 2024-01-19 criteria provided, single submitter clinical testing

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