ClinVar Miner

Submissions for variant NM_024675.3(PALB2):c.2391del (p.Gln797fs) (rs1555460360)

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Total submissions: 3
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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 RCV000210140 SCV000266104 pathogenic Hereditary cancer-predisposing syndrome 2015-11-20 criteria provided, single submitter clinical testing
Cancer Genetics Laboratory,Peter MacCallum Cancer Centre RCV000114525 SCV000267968 likely pathogenic Familial cancer of breast 2015-06-01 criteria provided, single submitter case-control
Leiden Open Variation Database RCV000114525 SCV001193222 pathogenic 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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