ClinVar Miner

Submissions for variant NM_139027.6(ADAMTS13):c.824+13C>T

gnomAD frequency: 0.00593  dbSNP: rs149586801
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000273167 SCV000478311 likely benign Upshaw-Schulman syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001613224 SCV001834890 benign not provided 2021-06-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001613224 SCV002395453 benign not provided 2025-01-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001613224 SCV005226042 likely benign not provided criteria provided, single submitter not provided

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