ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1140+10T>C

dbSNP: rs1060504332
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000580983 SCV000684113 likely benign Hereditary cancer-predisposing syndrome 2017-02-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001454576 SCV001658308 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2023-10-18 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004787759 SCV005407172 likely benign Familial cancer of breast 2024-08-23 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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