ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.168C>T (p.Gly56=)

dbSNP: rs2149014882
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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 RCV001921462 SCV002200506 likely benign Duchenne muscular dystrophy 2025-01-30 criteria provided, single submitter clinical testing

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