ClinVar Miner

Submissions for variant NM_004380.3(CREBBP):c.4332C>T (p.Cys1444=)

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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 RCV002611254 SCV003503478 likely benign Rubinstein-Taybi syndrome 2023-06-25 criteria provided, single submitter clinical testing

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