ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.425+33A>G (rs200065709)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000503983 SCV000591677 likely benign not specified criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory,University Medical Center Utrecht RCV000211021 SCV000743238 benign Breast-ovarian cancer, familial 2 2014-10-09 criteria provided, single submitter clinical testing
Michigan Medical Genetics Laboratories,University of Michigan RCV000211021 SCV000195948 benign Breast-ovarian cancer, familial 2 2014-11-03 criteria provided, single submitter clinical testing

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