ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.2586+81C>T

gnomAD frequency: 0.00885  dbSNP: rs114710547
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001566290 SCV001789788 likely benign not provided 2018-06-26 criteria provided, single submitter clinical testing
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002225303 SCV002504926 benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003315618 SCV004016500 likely benign Breast-ovarian cancer, familial, susceptibility to, 5 2023-07-07 criteria provided, single submitter clinical testing
Leiden Open Variation Database RCV001030325 SCV001193254 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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