ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.3114-51=

gnomAD frequency: 0.99999  dbSNP: rs249936
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001650947 SCV001864469 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Leiden Open Variation Database RCV001030385 SCV001193353 likely benign Familial cancer of breast 2019-05-13 no assertion criteria provided curation Curators: Marc Tischkowitz, Arleen D. Auerbach. Submitter to LOVD: Marc Tischkowitz.
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute RCV001689642 SCV001905928 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001689642 SCV001951226 benign not specified no assertion criteria provided clinical testing

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