ClinVar Miner

Submissions for variant NM_139027.6(ADAMTS13):c.961G>C (p.Ala321Pro)

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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 RCV005045953 SCV005681494 uncertain significance Upshaw-Schulman syndrome 2024-06-03 criteria provided, single submitter clinical testing

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