ClinVar Miner

Submissions for variant NM_004380.3(CREBBP):c.4992C>G (p.Arg1664=)

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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 RCV003760168 SCV004513275 likely benign Rubinstein-Taybi syndrome 2023-01-30 criteria provided, single submitter clinical testing

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