ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.517-2A>C

dbSNP: rs81002858
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Sharing Clinical Reports Project (SCRP) RCV000144186 SCV000189259 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 2 2014-01-02 no assertion criteria provided clinical testing

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