ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1141-14C>A

dbSNP: rs2077954619
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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 RCV001185041 SCV001351171 likely benign Hereditary cancer-predisposing syndrome 2019-03-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002559076 SCV003323198 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2022-03-11 criteria provided, single submitter clinical testing

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