ClinVar Miner

Submissions for variant NM_003579.4(RAD54L):c.267T>G (p.Tyr89Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV004764674 SCV005374270 likely pathogenic Lymphoma, non-Hodgkin, familial 2024-09-22 criteria provided, single submitter clinical testing

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