ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2258-15T>C

gnomAD frequency: 0.00002  dbSNP: rs780573511
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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 RCV001177569 SCV001341801 likely benign Hereditary cancer-predisposing syndrome 2019-12-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068196 SCV002324510 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-11-30 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004789415 SCV005405786 likely benign Familial cancer of breast 2024-09-04 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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