ClinVar Miner

Submissions for variant NM_007289.4(MME):c.1833T>C (p.Ser611=)

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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 RCV003053795 SCV003330877 likely benign not provided 2022-03-28 criteria provided, single submitter clinical testing

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