ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.2955T>C (p.Ser985=)

dbSNP: rs765643734
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001189109 SCV001356313 likely benign Hereditary cancer-predisposing syndrome 2020-03-21 criteria provided, single submitter clinical testing
Invitae RCV001476693 SCV001680905 likely benign Familial cancer of breast 2020-07-23 criteria provided, single submitter clinical testing
Leiden Open Variation Database RCV001030358 SCV001193315 uncertain significance not provided 2018-10-10 no assertion criteria provided curation Curators: Marc Tischkowitz, Arleen D. Auerbach. Submitter to LOVD: Yukihide Momozawa.

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