ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.1468C>T (p.Pro490Ser)

dbSNP: rs878855101
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000581576 SCV000690788 uncertain significance Hereditary cancer-predisposing syndrome 2018-08-11 criteria provided, single submitter clinical testing
Leiden Open Variation Database RCV001030232 SCV001193110 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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