ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.6757C>G (p.Leu2253Val) (rs1555284846)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory,University Medical Center Utrecht RCV000624985 SCV000743323 likely benign Breast-ovarian cancer, familial 2 2017-07-28 criteria provided, single submitter clinical testing
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000624985 SCV000744500 likely benign Breast-ovarian cancer, familial 2 2015-09-21 criteria provided, single submitter clinical testing

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