ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7008-1G>A (rs786204280)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario RCV000168595 SCV000219387 likely pathogenic Breast and/or ovarian cancer 2015-09-02 criteria provided, single submitter clinical testing
Color RCV000582155 SCV000689022 likely pathogenic Hereditary cancer-predisposing syndrome 2018-08-27 criteria provided, single submitter clinical testing
Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA), c/o University of Cambridge RCV000258461 SCV000327574 pathogenic Breast-ovarian cancer, familial 2 2015-10-02 criteria provided, single submitter clinical testing

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