ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.3114-42G>T

gnomAD frequency: 0.00004  dbSNP: rs515726106
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Washington Department of Laboratory Medicine, University of Washington RCV000208880 SCV000265343 likely benign Hereditary cancer-predisposing syndrome 2015-12-01 no assertion criteria provided clinical testing
Leiden Open Variation Database RCV001030386 SCV001193354 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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