ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.8364G>C (p.Trp2788Cys)

dbSNP: rs397507981
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Research Molecular Genetics Laboratory, Women's College Hospital, University of Toronto RCV000496368 SCV000587950 uncertain significance not specified 2014-01-31 no assertion criteria provided research

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