ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.86T>G (p.Leu29Arg)

dbSNP: rs1135401889
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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 RCV000496931 SCV000587537 uncertain significance not specified 2014-01-31 no assertion criteria provided research

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