ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1795-12_1795-10del

dbSNP: rs1475317357
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000557738 SCV000633567 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-01-17 criteria provided, single submitter clinical testing
GeneDx RCV001712768 SCV000721964 likely benign not provided 2023-03-07 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Color Diagnostics, LLC DBA Color Health RCV001184256 SCV001350201 likely benign Hereditary cancer-predisposing syndrome 2017-10-27 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003492092 SCV004240387 uncertain significance Breast and/or ovarian cancer 2023-04-25 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004787866 SCV005404502 likely benign Familial cancer of breast 2024-08-29 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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