ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.3792T>C (p.Val1264=)

dbSNP: rs2148222947
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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 RCV001461802 SCV001665710 likely benign Duchenne muscular dystrophy 2024-03-18 criteria provided, single submitter clinical testing

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