ClinVar Miner

Submissions for variant NM_004380.3(CREBBP):c.7005C>T (p.Ile2335=)

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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 RCV002596899 SCV002942089 likely benign Rubinstein-Taybi syndrome 2022-09-12 criteria provided, single submitter clinical testing

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