ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.1684+18TGA[7]

dbSNP: rs368593832
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003321504 SCV004027083 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Leiden Open Variation Database RCV001030247 SCV001193139 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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