ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.2548T>C (p.Trp850Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Human Genetics, Hannover Medical School RCV004574933 SCV005050116 uncertain significance Episodic pain syndrome, familial, 2 2024-06-10 criteria provided, single submitter clinical testing

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