ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.-39-26G>A

dbSNP: rs1566214447
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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 RCV000735544 SCV000863682 benign Breast and/or ovarian cancer 2013-02-15 no assertion criteria provided clinical testing

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