ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.507+67T>C

gnomAD frequency: 0.03383  dbSNP: rs73991950
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001671215 SCV001885210 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002225906 SCV002505048 benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001671215 SCV005252923 benign not provided criteria provided, single submitter not provided

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