ClinVar Miner

Submissions for variant NM_005475.3(SH2B3):c.1566dup (p.Glu523fs)

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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 RCV003990125 SCV004806454 likely pathogenic Primary myelofibrosis 2024-03-25 criteria provided, single submitter clinical testing

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