ClinVar Miner

Submissions for variant NM_001079668.3(NKX2-1):c.1025del (p.Gly342fs)

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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 RCV003237310 SCV003935973 likely pathogenic Benign hereditary chorea 2020-03-10 criteria provided, single submitter clinical testing

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