ClinVar Miner

Submissions for variant NM_139027.6(ADAMTS13):c.270C>T (p.Pro90=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003861087 SCV004667180 likely benign not provided 2023-05-16 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005040583 SCV005681452 uncertain significance Upshaw-Schulman syndrome 2024-02-20 criteria provided, single submitter clinical testing

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