ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.5087G>T (p.Gly1696Val)

dbSNP: rs1135401904
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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 RCV000496779 SCV000587743 pathogenic Hereditary breast ovarian cancer syndrome 2014-01-31 no assertion criteria provided research

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