ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5468-11T>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomics and Molecular Medicine Service, East Genomic Laboratory Hub, NHS Genomic Medicine Service RCV004584299 SCV005068354 uncertain significance Inherited breast cancer and ovarian cancer 2024-04-17 criteria provided, single submitter clinical testing BP4

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