ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.380-18_380-17dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV004788889 SCV005405677 benign Familial cancer of breast 2024-08-21 criteria provided, single submitter clinical testing This variant is considered benign. This variant is intronic and is not expected to impact mRNA splicing.

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