ClinVar Miner

Submissions for variant NM_139025.4(ADAMTS13):c.-357T>C

gnomAD frequency: 0.07895  dbSNP: rs34265876
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000289469 SCV000478297 likely benign Upshaw-Schulman syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001653751 SCV001865257 benign not provided 2021-06-18 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001653751 SCV005226036 likely benign not provided criteria provided, single submitter not provided

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