ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.2098-10C>T

dbSNP: rs864622767
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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 RCV000580555 SCV000684184 likely benign Hereditary cancer-predisposing syndrome 2017-02-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001411207 SCV001613266 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-12-02 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004791329 SCV005405199 likely benign Familial cancer of breast 2024-09-03 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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