ClinVar Miner

Submissions for variant NM_001069.3(TUBB2A):c.528A>C (p.Ser176=)

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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 RCV002592047 SCV003499999 likely benign not provided 2022-10-26 criteria provided, single submitter clinical testing

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