ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1980C>T (p.Leu660=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005226420 SCV005864727 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2025-01-23 criteria provided, single submitter clinical testing

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