ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.3294G>A (p.Lys1098=)

dbSNP: rs875989796
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cancer Genetics Laboratory, Peter MacCallum Cancer Centre RCV000211069 SCV000268035 likely benign Familial cancer of breast 2015-06-01 criteria provided, single submitter case-control

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