ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1340+19T>C

dbSNP: rs2077944993
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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 RCV001182104 SCV001347455 likely benign Hereditary cancer-predisposing syndrome 2018-12-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068306 SCV002479635 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-02-09 criteria provided, single submitter clinical testing

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