ClinVar Miner

Submissions for variant NM_139027.6(ADAMTS13):c.463T>C (p.Cys155Arg)

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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 RCV005045934 SCV005681459 uncertain significance Upshaw-Schulman syndrome 2024-05-24 criteria provided, single submitter clinical testing

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