ClinVar Miner

Submissions for variant NM_000077.5(CDKN2A):c.*29G>C

gnomAD frequency: 0.85710  dbSNP: rs11515
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001655674 SCV001867334 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001655674 SCV005271887 benign not provided criteria provided, single submitter not provided
Faculté Pluridciplinaire Nador, Université Mohamed Premier RCV001250946 SCV001250929 uncertain significance Squamous cell lung carcinoma 2020-05-05 no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001529165 SCV001742173 benign not specified no assertion criteria provided clinical testing
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute RCV001529165 SCV001905681 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001529165 SCV001957729 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001529165 SCV001964405 benign not specified no assertion criteria provided clinical testing

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