ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.9195T>A (p.Phe3065Leu) (rs80359179)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000709339 SCV000838898 uncertain significance Hereditary breast and ovarian cancer syndrome 2018-07-02 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000031802 SCV000054410 uncertain significance Breast-ovarian cancer, familial 2 2009-12-02 no assertion criteria provided clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000031802 SCV000147564 uncertain significance Breast-ovarian cancer, familial 2 2002-05-29 no assertion criteria provided clinical testing

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