ClinVar Miner

Submissions for variant NM_007289.4(MME):c.1452T>C (p.Asp484=)

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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 RCV003573991 SCV004332152 likely benign not provided 2023-10-11 criteria provided, single submitter clinical testing

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