ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.3767A>C (p.His1256Pro) (rs80358618)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000561816 SCV000668598 uncertain significance Hereditary cancer-predisposing syndrome 2019-07-15 criteria provided, single submitter clinical testing Insufficient or conflicting evidence
Mendelics RCV000113216 SCV001139071 likely benign Breast-ovarian cancer, familial 2 2019-05-28 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113216 SCV000146294 uncertain significance Breast-ovarian cancer, familial 2 2002-05-29 no assertion criteria provided clinical testing

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