ClinVar Miner

Submissions for variant NM_001363711.2(DUOX2):c.4157del (p.Gly1386fs)

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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 RCV005009644 SCV005637777 likely pathogenic Thyroid dyshormonogenesis 6 2024-05-20 criteria provided, single submitter clinical testing

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