ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.2566C>T (p.Gln856Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Medical Genetics, National & Kapodistrian University of Athens RCV002470687 SCV002769580 likely pathogenic Duchenne muscular dystrophy 2022-12-16 criteria provided, single submitter clinical testing PVS1,PM2

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