ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.48_50delinsAAT (p.Thr17Ile)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003740562 SCV004562733 uncertain significance not provided 2023-10-06 criteria provided, single submitter clinical testing

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