ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.527_530del (p.Thr176fs) (rs1566219179)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research RCV000735561 SCV000863699 pathogenic Breast and/or ovarian cancer 2012-03-28 no assertion criteria provided clinical testing

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