ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.2827G>C (p.Glu943Gln)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003993348 SCV004810619 uncertain significance not provided 2024-03-01 criteria provided, single submitter clinical testing PALB2: PM2
Baylor Genetics RCV004573449 SCV005053858 uncertain significance Familial cancer of breast 2024-03-24 criteria provided, single submitter clinical testing

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