ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.1585_1586insA (p.Phe529fs)

dbSNP: rs1135401893
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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 RCV000496932 SCV000587600 pathogenic Hereditary breast ovarian cancer syndrome 2014-01-31 no assertion criteria provided research

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