ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1628+15C>T

dbSNP: rs751454994
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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 RCV000775420 SCV000909775 likely benign Hereditary cancer-predisposing syndrome 2018-08-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003768387 SCV004573782 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2025-01-08 criteria provided, single submitter clinical testing

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