ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.2835-27C>T

gnomAD frequency: 0.00079  dbSNP: rs199757736
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002225304 SCV002504922 likely benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002267853 SCV002551647 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704850 SCV005213517 likely benign not provided criteria provided, single submitter not provided
Leiden Open Variation Database RCV001030353 SCV001193302 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.

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