ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.3916C>T (p.Leu1306=)

dbSNP: rs1251778900
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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 RCV002080853 SCV002374183 likely benign Duchenne muscular dystrophy 2021-10-21 criteria provided, single submitter clinical testing

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