ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1936-7A>T

gnomAD frequency: 0.00001  dbSNP: rs1427111542
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000937471 SCV001083256 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-01-28 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001731983 SCV001983672 uncertain significance not specified 2021-09-16 criteria provided, single submitter clinical testing

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