ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.8633-26A>G (rs56268579)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000045582 SCV000073595 benign Hereditary breast and ovarian cancer syndrome 2020-08-05 criteria provided, single submitter clinical testing
Michigan Medical Genetics Laboratories,University of Michigan RCV000113976 SCV000267821 benign Breast-ovarian cancer, familial 2 2016-04-21 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000501105 SCV000592216 likely benign not specified 2017-10-25 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113976 SCV000147422 uncertain significance Breast-ovarian cancer, familial 2 2002-06-27 no assertion criteria provided clinical testing

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