ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.206-14T>A

dbSNP: rs914741353
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000773699 SCV000907398 likely benign Hereditary cancer-predisposing syndrome 2023-04-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067272 SCV002431075 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2025-01-05 criteria provided, single submitter clinical testing

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