ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.1299G>T (p.Leu433Phe)

dbSNP: rs1966978476
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine RCV001258208 SCV001435103 uncertain significance Pancreatic cancer, susceptibility to, 3; Breast cancer, susceptibility to criteria provided, single submitter clinical testing

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