ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.8276T>C (p.Val2759Ala)

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Total submissions: 1
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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 RCV003493306 SCV004240363 uncertain significance Breast and/or ovarian cancer 2022-12-16 criteria provided, single submitter clinical testing

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