ClinVar Miner

Submissions for variant NM_004958.4(MTOR):c.6678T>C (p.Ala2226=)

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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 RCV002741856 SCV003022207 likely benign not provided 2023-02-16 criteria provided, single submitter clinical testing

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