ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2492+15del

dbSNP: rs2061852353
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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 RCV001188381 SCV001355436 likely benign Hereditary cancer-predisposing syndrome 2019-04-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005225296 SCV005866998 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-03-11 criteria provided, single submitter clinical testing

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