ClinVar Miner

Submissions for variant NM_003235.5(TG):c.1830_1831del (p.Gln610fs)

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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 RCV005048277 SCV005680156 likely pathogenic Iodotyrosyl coupling defect; Autoimmune thyroid disease, susceptibility to, 3 2024-02-15 criteria provided, single submitter clinical testing

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