ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2905+17C>T

dbSNP: rs1458780264
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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 RCV000777021 SCV000912700 likely benign Hereditary cancer-predisposing syndrome 2017-12-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002535591 SCV003258754 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-02-02 criteria provided, single submitter clinical testing

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