ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1935+13T>G

dbSNP: rs1555602100
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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 RCV000582102 SCV000689294 likely benign Hereditary cancer-predisposing syndrome 2015-12-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061774 SCV002338869 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-10-07 criteria provided, single submitter clinical testing

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