ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.2587-38C>G

gnomAD frequency: 0.00082  dbSNP: rs180177119
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002267852 SCV002551655 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Leiden Open Variation Database RCV001030328 SCV001193257 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 RCV001682801 SCV001905686 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001682801 SCV001951194 likely benign not provided no assertion criteria provided clinical testing

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