ClinVar Miner

Submissions for variant NM_001079668.3(NKX2-1):c.822C>A (p.Cys274Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostics Lab, Nemours Children's Health, Delaware RCV003237295 SCV003935949 likely pathogenic Brain-lung-thyroid syndrome 2020-02-11 criteria provided, single submitter clinical testing

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