ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.93+8T>C

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV004788892 SCV005405689 likely benign Familial cancer of breast 2024-08-09 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.
Labcorp Genetics (formerly Invitae), Labcorp RCV005221071 SCV005863648 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-10-28 criteria provided, single submitter clinical testing

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