ClinVar Miner

Submissions for variant NM_004380.3(CREBBP):c.7282G>C (p.Gly2428Arg)

dbSNP: rs761138453
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579925 SCV001809059 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001579925 SCV001969985 uncertain significance not provided no assertion criteria provided clinical testing

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