ClinVar Miner

Submissions for variant NM_015175.3(NBEAL2):c.7460_7461del (p.Thr2487fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Immunogenetics of Pediatric Autoimmune Diseases, Institut Imagine RCV003151928 SCV003840225 pathogenic Gray platelet syndrome no assertion criteria provided research

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