ClinVar Miner

Submissions for variant NM_005572.4(LMNA):c.1714C>G (p.Arg572Gly)

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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 RCV005088761 SCV005720442 likely benign Charcot-Marie-Tooth disease type 2 2024-05-05 criteria provided, single submitter clinical testing

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