ClinVar Miner

Submissions for variant NM_001363711.2(DUOX2):c.4052del (p.Lys1351fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005009645 SCV005637779 likely pathogenic Thyroid dyshormonogenesis 6 2024-04-24 criteria provided, single submitter clinical testing

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