ClinVar Miner

Submissions for variant NM_004380.3(CREBBP):c.57G>T (p.Ser19=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005101674 SCV005812918 benign Rubinstein-Taybi syndrome 2024-11-25 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003904306 SCV004725127 likely benign CREBBP-related disorder 2024-02-19 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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