ClinVar Miner

Submissions for variant NM_001206744.2(TPO):c.1339-1147T>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003610001 SCV004564296 benign Deficiency of iodide peroxidase 2023-11-06 criteria provided, single submitter clinical testing

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